Y-DNA haplogroups in populations of Central and North Asia
Appearance
Research into the predominant human Y-DNA haplogroups of Central Asia and Siberia, broken down according to both individual publications and ethnolinguistic groups, are summarized in the table below.
The first two columns of the table list ethnicity and linguistic affiliations, the third column cites the total sample size in each study, and the adjoining columns give the percentage of each haplogrou or subclade found sample in a particular sample.
Population | Language | n | C | I | J | K* | N | O3 | P* | Q | R1a | R1b/R1* | R2 | Others | Reference |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Altaians | Turkic | 98 | 22.4 | 0 | 3.0 | 17.3 | 46.9 | 0 | Tambets 2004[1] | ||||||
Altaians | Turkic | 92 | 13.0 | 2.2 | 2.2 | 0 | 7.6 | 28.3 | 41.3 | 1.1 | D = 3 | Derenko 2005[2] | |||
Altaians (northern) | Turkic | 50 | 0 | 2 | 10 | 38 | 6 | Kharkov 07[3] | |||||||
Altaians (southern) | Turkic | 96 | 2.1 | 4.2 | 11.5 | 53.1 | 1 | E = 1 | Kharkov 2007[3] | ||||||
Buryats | Mongolic | 238 | 63.9 | 0.4 | 0 | 8.8 | 20.2 | 1.7 | 1.7 | 2.1 | 0.8 | G = 0.4 | Derenko 2005[2] | ||
Chukchis | Chukotkan | 24 | 4.2 | 0 | 0 | 0 | 58.3 | 0 | 20.8 | 15.5 | 4.2 | 0 | 0 | 0 | Lell 2001[4] |
Dolgans | Turkic | 67 | 37.3 | 1.5 | 34.1 | 16.4 | 1.5 | Tambets 2004[1] | |||||||
Dungans | Sino-Tibetan | 40 | 2.5 | 12.5 | 2.5 | 2.5 | 40 | 0 | 7.5 | 10 | 5 | 5 | O1 = 5; F(xIJ) = 5 (possibly F(xGHIJK), G, H, or LT) | Wells 2001[5] | |
Evens | Tungusic | 31 | 74.2 | 3.2 | 12.9 | 0 | 6.5 | 0 | Tambets 2004[1] | ||||||
Evenks | Tungusic | 96 | 67.7 | 5.2 | 19.8 | 4.2 | 1 | 0 | Tambets 2004[1] | ||||||
Itelmens | Kamchatkan | 18 | 67 | 0 | 0 | 0 | 11 | 0 | 0 | 0 | 22 | 0 | 0 | 0 | Lell 2001[4] |
Kalmyks | Mongolic | 68 | 70.6 | 0 | 0 | 4.4 | 2.9 | 11.8 | 5.9 | 2.9 | L = 1.5 | Derenko 2005[2] | |||
Karakalpaks | Turkic | 44 | 22.7 | 0 | 9.1 | 6.8 | 2.3 | 11.4 | 0 | 0 | 18.2 | 9.1 | 6.8 | F(xIJ) = 9 (possibly F(xGHIJK), G, or H); L = 5 |
Wells 2001[5] |
Kazakhs | Turkic | 54 | 66.7 | 0 | 0 | 0 | 1.9 | 9.3 | 5.6 | 0 | 3.7 | 5.6 | 1.9 | D = 2, F(xIJ) = 2 (possibly F(xGHIJK), G, or H) | Wells 2001[5] |
Kazakhs | Turkic | 30 | 40 | 13.3 | 10 | 10 | 3.3 | 6.7 | F(xIJ) = 17 (possibly F(xGHIJK), G, H, or LT) | Karafet 2001[6] | |||||
Kazakhs (Altai Republic) |
Turkic | 119 | 59.7 (C3) |
0 | 4.2 | 0 | 0 | 26.1 | 0 | 0.8 | 0.8 | 2.5 | 0 | G = 5, T = 0.8 | Dulik 2011[7] |
Kets | Dené–Yeniseian | 48 | 6.2 | 0 | 0 | 0 | 0 | 0 | 93.7 | 0 | 0 | 0 | 0 | Tambets 2004[1] | |
Khakas | Turkic | 53 | 5.7 | 3.8 | 0 | 5.7 | 41.5 | 7.6 | 28.3 | 7.6 | Derenko 2005[2] | ||||
Khants | Uralic | 47 | 0 | 0 | 0 | 0 | 76.6 | 0 | 0 | 0 | 4.3 | 19.1 | 0 | 0 | Tambets 2004[1] |
Koryaks | Chukotkan | 27 | 59.2 | 0 | 0 | 0 | 22.2 | 0 | 18.5 | 0 | 0 | 0 | 0 | 0 | Lell 2001[4] |
Kyrgyz | Turkic | 52 | 13.5 | 1.9 | 1.9 | 1.9 | 1.9 | 1.9 | 1.9 | 0 | 63.5 | 1.9 | 0 | O1 = 5.8 | Wells 2001[5] |
Mongolians | Mongolic | 65 | 53.8 | 3.1 | 1.5 | 10.8 | 10.8 | 4.6 | 9.2 | D = 1.5, O2 = 1.5 | Xue 2006[8] | ||||
Nenets | Uralic | 148 | 0 | 0 | 97.3 | 1.4 | 0 | 0 | Tambets 2004[1] | ||||||
Nganasans | Uralic | 38 | 5.3 | 0 | 92.1 | 0 | 0 | Tambets 2004[1] | |||||||
Nivkhs | Nivkh (isolate) | 17 | 47 | 35 | Lell 2001[4] | ||||||||||
Romanis (Uzbekistan) | Indo-European | 15 | 0 | 0 | 20 | 0 | 0 | 7 | 0 | 0 | 0 | 0 | 53 | H = 13 | Wells 2001[5] |
Selkups | Uralic | 131 | 1.5 | 0 | 6.9 | 66.4 | 19.1 | 6.1 | Tambets 2004[1] | ||||||
Shors | Turkic | 51 | 2 | 0 | 0 | 0 | 15.7 | 0 | 2 | 0 | 58.8 | 19.6 | 0 | F(xIJ) = 2 (however, this study did not test – in accordance with later definitions – for subclades of F, such as H2, K2*, NO(xN1c1), Q(xQ-M3), P*, P1, R(xR1), or T).[2] | Derenko 2005[2] |
Tajiks | Indo-European | 38 | 2.6 | 0 | 18.4 | 0 | 0 | 0 | 0 | 0 | 44.7 | 0 | 7.9 | L = 8, H = 5, E = 3 |
Wells 2001[5] |
Teleuts | Turkic | 47 | 8.5 | 4.3 | 2.1 | 0 | 10.6 | 0 | 55.3 | 12.8 | F(xIJ) = 6.4% (however, this study did not test – in accordance with later definitions – for subclades of F, such as H2, K2*, NO(xN1c1), Q(xQ-M3), P*, P1, R(xR1), or T).[2] |
Derenko 2005[2] | |||
Tofalars | Turkic | 32 | 6.3 | 3.1 | 0 | 3.1 | 59.4 | 0 | 3.1 | 0 | 12.5 | 12.5 | 0 | 0 | Derenko 2005[2] |
Turkmens | Turkic | 30 | 0 | 0 | 17 | 13 | 0 | 0 | 10 | 0 | 7 | 37 | 3 | F(xIJ) = 13 (most likely G or H) | Wells 2001[5] |
Tuvans | Turkic | 113 | 7.1 | 0.9 | 0 | 8.9 | 23.9 | 35.4 | 17.7 | G = 0.9; F(xIJ) = 3.5 (however, this study did not test – in accordance with later definitions – for subclades of F, such as H2, K2*, NO(xN1c1), Q(xQ-M3), P*, P1, R(xR1), or T).[2] | Derenko 2005[2] | ||||
Tuvans | Turkic | 108 | 38.0 | 1.9 (R-M73) |
0 | Malyarchuk 2011[9] | |||||||||
Uyghurs | Turkic | 70 | 4.3 | 11.4 | 7.1 | 8.6 | 11.4 | (see "Others") | (see "Others") | 18.6 | (see "Others") | (see "Others") | P(xR1a) = 17.1 (probably P1, Q, R1b or R2) | Xue 2006[8] | |
Uyghurs | Turkic | 67 | 7.5 | 10.4 | 6.0 | 10.5 | 3.0 | (see "Others") | (see "Others") | (see "Others") | D3 = 4.5, G = 4.5, L = 4.5, R = 46.3 (probably R1a, R1b or R2) |
Hammer 2005 [10] | |||
Uyghurs | Turkic | 187 (four samples) | 5.3 | 0.35 | 15.7 | 5.0 | (see "Others") | 6.78 | 21.6 | 6.7 | 2.6 | D = 3.75, E= 2.1, G = 1.5, H = 3.15, L = 3.8, O(xO3) = 16.2, T = 0.5 |
Zhong 2010 [11] | ||
Uzbeks | Turkic | 366 | 11.5 | 2.2 | 13.4 | 6.8 | 1.4 | 4.1 | 5.5 | 0 | 25.1 | 9.8 | 2.2 | F(xIJK) = 7.9 (most likely G or H), L = 3, E = 2, D = 2 |
Wells 2001[5] |
Yaghnobis | Indo-European | 31 | 3 | 0 | 32 | 3 | 0 | 0 | 3 | 0 | 16 | 32 | 0 | L = 10 | Wells 2001[5] |
Yakuts | Turkic | 155 | 3.2 | 1.3 | 88.4 | 0 | 1.9 | 1.9 | Tambets 2004[1] | ||||||
Yukaghir | Yukaghir | 13 | 31 (C3) |
0 | 0 | 0 | 31 | 0 | 0 | 31 | 0 | 0 | 0 | F(xIJ) = 8 (possibly F(xGHIJK), G or H) | Duggan 2013[12] |
Yupik | Eskimo–Aleut | 33 | 0 | 50.6 | 0 | 18.2 | 21.2 | 0 | Lell 2001[4] |
See also
- Demography of Central Asia
- Indigenous peoples of Siberia
- Y-DNA haplogroups by groups
- Y-DNA haplogroups by populations of the Caucasus
- Y-DNA haplogroups in South Asian populations
- Y-DNA haplogroups by populations of East and Southeast Asia
- Y-DNA haplogroups by populations of Near East and North Africa
- Y-DNA haplogroups in European populations
- Y-DNA haplogroups in Oceanian populations
- Y-DNA haplogroups by populations of Sub-Saharan Africa
- Y-DNA haplogroups in Indigenous peoples of the Americas
References
- ^ a b c d e f g h i j Tambets, Kristiina et al. 2004, The Western and Eastern Roots of the Saami—the Story of Genetic “Outliers” Told by Mitochondrial DNA and Y Chromosomes
- ^ a b c d e f g h i j k Miroslava Derenko et al. 2005, Contrasting patterns of Y-chromosome variation in South Siberian populations from Baikal and Altai-Sayan regions
- ^ a b Khar'kov, VN; Stepanov, VA; Medvedeva, OF; Spiridonova, MG; Voevoda, MI; Tadinova, VN; Puzyrev, VP (2007). "Gene pool differences between Northern and Southern Altaians inferred from the data on Y-chromosomal haplogroups". Genetika. 43 (5): 675–87. PMID 17633562.
- ^ a b c d e Lell, Jeffrey T. et al. 2001-2002, The Dual Origin and Siberian Affinities of Native American Y Chromosomes
- ^ a b c d e f g h i Wells, Spencer et al. 2001, The Eurasian Heartland: A continental perspective on Y-chromosome diversity
- ^ Karafet Tatiana et al. 2001, Paternal Population History of East Asia: Sources, Patterns, and Microevolutionary Processes
- ^ Dulik, Matthew C. et al. 2011, Y-Chromosome Variation in Altaian Kazakhs Reveals a Common Paternal Gene Pool for Kazakhs and the Influence of Mongolian Expansions
- ^ a b Xue, Yali et al. 2006 Male demography in East Asia: a north-south contrast in human population expansion times Archived September 6, 2008, at the Wayback Machine
- ^ Malyarchuk, Boris et al. 2011, Ancient links between Siberians and Native Americans revealed by subtyping the Y chromosome haplogroup Q1a Archived November 3, 2013, at the Wayback Machine Journal of Human Genetics (2011) 56, 583–588
- ^ Michael F Hammer et al. 2005, Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes Journal of Human Genetics (2006) 51, 47–58; doi:10.1007/s10038-005-0322-0
- ^ Hua Zhong et al., 2010, "Extended Y-chromosome investigation suggests post-Glacial migrations of modern humans into East Asia via the northern route", Mol Biol Evol, doi: 10.1093/molbev/msq247.
- ^ Duggan AT, Whitten M, Wiebe V, Crawford M, Butthof A, et al. (2013) Investigating the Prehistory of Tungusic Peoples of Siberia and the Amur-Ussuri Region with Complete mtDNA Genome Sequences and Y-chromosomal Markers PLoS ONE 8(12): e83570. doi:10.1371/journal.pone.0083570