dbVar has generated known structural variants (SV) datasets for use in comparisons with user data to aid variant calling, analysis and interpretation.
Files containing Non-Redundant (NR) deletions, insertions, and duplications are now available on GitHub. Additional separate files include preliminary annotations of overlap with ACMG59 genes. All files are in tab-delimited text format.
We encourage you to test these files and provide feedback, either on GitHub or by email.