Examples: RP11-34P13; CFTR, 7q11.21; chr7:71890181-72690180 Find DGV Variants. by Study: by Sample: by Method: by Variant: by Platform

May 15, 2016 · Over the past decade, the Database of Genomic Variants (DGV; http://dgv.tcag.ca/) has provided a publicly accessible, comprehensive curated catalogue of structural variation (SV) found in the genomes of control individuals from worldwide populations.

The DGV Structural Variation track contains the current and most up to date content in the database. The DGV Version 1 data is an older, archived copy of the content that was hosted on our original site (projects.tcag.ca/variation).

Over the past decade, the Database of Genomic Variants (DGV; http://dgv.tcag.ca/) has provided a publicly accessible, comprehensive curated catalogue of structural variation (SV) found in the genomes of control individuals from worldwide populations.

Studies included in DGV and links to the original data. The table below outlines the studies that have been used as sources for the data and the number of regions included from each study. Here you can also download the original dataset for all studies.

dbVar is NCBI's database of human genomic Structural Variation — large variants >50 bp including insertions, deletions, duplications, inversions, mobile elements, translocations, and complex variants. Announcing the dbVar Public Track Hub! dbVar has released a track hub containing curated datasets of Clinical SV and Common SV.

Over the past decade, the Database of Genomic Variants (DGV; http://dgv.tcag.ca/) has provided a publicly accessible, comprehensive curated catalogue of structural variation (SV) found in the genomes of control individuals from worldwide populations.

The Database of Genomic Variants archive (DGVa) is a repository that provides archiving, accessioning and distribution of publicly available genomic structural variants, in all species.

This track displays 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.