The Genome Variation Map (GVM) is a public data repository of genome variations, including single nucleotide polymorphisms and small insertions and deletions, with particular focuses on human as well as cultivated plants and domesticated animals.
All species with genomic variants
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How to Cite

When you have successfully submitted data to GVM, please consider to use the following words to describe data deposition in your manuscript.

The variation data reported in this paper has been deposited in the Genome Variation Map [1] in National Genomics Data Center [2], China National Center for Bioinformation / Beijing Institute of Genomics, Chinese Academy of Sciences, under accession number GVMXXXXXX that can be publicly accessible at

1. Genome Variation Map: a data repository of genome variations in BIG Data Center. Nucleic Acids Res 2018, 46(D1):D944-D949.[PMID=29069473].
2. Database Resources of the National Genomics Data Center in 2020. Nucleic Acids Res 2020, 48(D1):D24-D33. [PMID=31702008].
3. GWAS Atlas: a curated resource of genome-wide variant-trait associations in plants and animals. Nucleic Acids Res 2020, 48(D1):D927-D932.[PMID=31566222].

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  A total of 27,849,593 SNPs and 2,137,083 Indels derived from 190 Capsicum annuum (Pepper) accessions are integrated into GVM (2020-08-20)

  A total of 21,396,685 SNPs derived from 36 Daucus carota (Carrot) accessions are integrated into GVM (2018-01-05)

  GVM is accepted by Nucleic Acids Res at 2017-10-10 (2017-10-19)