The tracks listed here contain data from the nstd186 (NCBI Curated Common Structural Variants) study. This is a collection of structural variants (SV) originally submitted to dbVar which are part of a study with at least 100 samples and have an allele frequency of >=0.01 in at least one population. The complete dataset is imported from these common-population studies:

gnomAD Structural Variants (nstd166): Catalog of SVs detected from the sequencing of the complete genome of 10,847 unrelated individuals from the GnomAD v2.1 release.

1000 Genomes Consortium Phase 3 Integrated SV (estd219): Structural variants of the 1000 Genomes project Phase 3 as reported in a separate article specifically dedicated to the analysis of SVs. Many of these data are identical to those reported in the estd214 study.

DECIPHER Common CNVs (nstd183): Consensus set of common population CNVs selected from high-resolution controls sets where frequency information is available.

There are two tracks in this collection:

• NCBI dbVar Curated Common Structural Variants (dbVar Common SV): Shows copy number variants calls (variants >=50 nucleotides) from the nstd186 study.
• NCBI dbVar Curated Conflict Variants (dbVar Conflict SV): Shows copy number variants from nstd186 (NCBI Curated Common Structural Variants) that overlap with nstd102 (Clinical Structural Variants).

To view the full description, click here.