Korean Variant Archive (KOVA): a reference database of genetic variations in the Korean population

• Published in: Scientific reports Vol. 7; no. 1; pp. 4287 - 9
• Main Authors: Lee, Sangmoon, Seo, Jihae, Park, Jinman, Nam, Jae-Yong, Choi, Ahyoung, Ignatius, Jason S., Bjornson, Robert D., Chae, Jong-Hee, Jang, In-Jin, Lee, Sanghyuk, Park, Woong-Yang, Baek, Daehyun, Choi, Murim
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 27.06.2017; Nature Publishing Group; Nature Portfolio
• Subjects: 45/23; 631/208/212/2166; 631/208/212/2301; Archives & records; Asian Continental Ancestry Group - genetics; Copy number; Databases, Genetic; DNA Copy Number Variations; Exome; Genetic diversity; Genetic Predisposition to Disease; Genetic Variation; Genetics; Genetics, Population; Genomes; Germ-Line Mutation; Humanities and Social Sciences; Humans; Minority & ethnic groups; multidisciplinary; Neoplasms - genetics; Polymorphism, Single Nucleotide; Population genetics; Republic of Korea; Science; Science (multidisciplinary); Republic of Korea
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-017-04642-4

Despite efforts to interrogate human genome variation through large-scale databases, systematic preference toward populations of Caucasian descendants has resulted in unintended reduction of power in studying non-Caucasians. Here we report a compilation of coding variants from 1,055 healthy Korean individuals (KOVA; Korean Variant Archive). The samples were sequenced to a mean depth of 75x, yielding 101 singleton variants per individual. Population genetics analysis demonstrates that the Korean population is a distinct ethnic group comparable to other discrete ethnic groups in Africa and Europe, providing a rationale for such independent genomic datasets. Indeed, KOVA conferred 22.8% increased variant filtering power in addition to Exome Aggregation Consortium (ExAC) when used on Korean exomes. Functional assessment of nonsynonymous variant supported the presence of purifying selection in Koreans. Analysis of copy number variants detected 5.2 deletions and 10.3 amplifications per individual with an increased fraction of novel variants among smaller and rarer copy number variable segments. We also report a list of germline variants that are associated with increased tumor susceptibility. This catalog can function as a critical addition to the pre-existing variant databases in pursuing genetic studies of Korean individuals.