Hello Everyone,
We are pleased to announce an update to the DGV tracks for the hg38 and hg19 human assemblies. The tracks display copy number variants (CNVs), insertions/deletions (InDels), inversions and inversion breakpoints annotated by the Database of Genomic Variants (DGV), which contains genomic variations observed in healthy individuals. For the hg38 update, the Structural Variant Regions track now has 825,343 total variants and the Supporting Structural Variants track now has 7,270,185 total variants. For the hg19 update, Structural Variant Regions track now has 826,661 total variants and the Supporting Structural Variants track now has 7,346,512 total variants. More information on these tracks can be found on the track description page.
We would like to thank the Database of Genomic Variants for making these data available. We would also like to thank Jairo Navarro, Max Haeussler, Anna Benet-Pages, and Gerardo Perez for their efforts on this release.