A catalogue of early diverged contemporary human genome variation reveals distinct Khoe-San populations

Creating a catalogue of early diverged genome variation is critical to determine the true extent of human diversity and associated medical impact. Generating deep whole genome data for 150 Khoe-San (12 groups, 1 unclassified), and 40 regionally comparative Southern Africans (3 groups), we identify ~30 million small-to-large variants - over 1.3 million unknown single nucleotide variants. Representing shared traditionally forager lifestyles and click-speaking languages, we identify San and Damara as separate phylogenetic lineages, contributing two admixture waves to Nama. While San represented modern humans' deep divergence (~115 thousand years ago), Damara divergence is recent, with both showing high effective population sizes between 45-150 thousand years ago. Developing an assembly-based test we report 1,376 genes under positive selection (dN/dS = 19.46) of which 479 are significantly associated with forager peoples and, therefore, maintained ancestral alleles that differ from derived genetic variation observed in non-African biomedical resources.

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Journal
Nature Communications
Published
2026-02-10
DOI
https://doi.org/10.1038/s41467-026-69269-4
Primary Topic
Forensic and Genetic Research
Type
article
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article

A catalogue of early diverged contemporary human genome variation reveals distinct Khoe-San populations

Desiree C. Petersen, Weerachai Jaratlerdsiri, Kathrine Elizabeth Theron, Krkavcová Eva et al.
Nature Communications
Forensic and Genetic Research
article

A catalogue of early diverged contemporary human genome variation reveals distinct Khoe-San populations

Desiree C. Petersen, Weerachai Jaratlerdsiri, Kathrine Elizabeth Theron, Krkavcová Eva, Vanessa Hayes, Jeffrey Mphahlele, Errol Holland, Pamela X. Y. Soh, Hagen E. A. Förtsch, Zolani Simayi, Jue Jiang, Wilfrid H. G. Haacke, David M. Thomas, M. S. Riana Bornman, Tingting Gong
article en

Abstract

Creating a catalogue of early diverged genome variation is critical to determine the true extent of human diversity and associated medical impact. Generating deep whole genome data for 150 Khoe-San (12 groups, 1 unclassified), and 40 regionally comparative Southern Africans (3 groups), we identify ~30 million small-to-large variants - over 1.3 million unknown single nucleotide variants. Representing shared traditionally forager lifestyles and click-speaking languages, we identify San and Damara as separate phylogenetic lineages, contributing two admixture waves to Nama. While San represented modern humans' deep divergence (~115 thousand years ago), Damara divergence is recent, with both showing high effective population sizes between 45-150 thousand years ago. Developing an assembly-based test we report 1,376 genes under positive selection (dN/dS = 19.46) of which 479 are significantly associated with forager peoples and, therefore, maintained ancestral alleles that differ from derived genetic variation observed in non-African biomedical resources.

Nature CommunicationsVol. 17(1)
Namibia University of Science and Technology (NA), South African Medical Research Council (ZA), University of East Anglia (GB), The University of Sydney (AU), New South Wales Department of Health (AU), University of Namibia (NA), Fudan University (CN), Stellenbosch University (ZA), North-West University (ZA), Sefako Makgatho Health Sciences University (ZA), UNSW Sydney (AU), Cancer Research UK Manchester Institute (GB), Namibia Institute of Pathology (NA), University of Pretoria (ZA), Neuroscience Research Australia (AU), University of Venda (ZA), University of Limpopo (ZA)
Openalex Percentile: Top 58%
Forensic and Genetic Research
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