dbVar is NCBI's database of human genomic structural variation — insertions, deletions, duplications, inversions, mobile elements, translocations, and others

Non-Redundant Structural Variation Datasets

江苏11选五开奖结果 www.nyms2.cn Would you like to compare and analyze your data with known structural variants (SV) in dbVar? Now there are easy-to-use files containing non-redundant (NR) deletions, duplications, and insertions aggregated from across studies in dbVar. The files are available for human assembly versions GRCh37 and GRCh38. Descriptions of the NR data and tutorials are available on GitHub.

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dbVar Webinar (Part 1 of 2)

dbVar Webinar (Part 2 of 2)

dbVar Data in Variation Viewer

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