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:
To view the full description, click here.
|