A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694858



Internal ID15431510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:117577743..117786463hg38UCSC Ensembl
Innerchr3:117296590..117505310hg19UCSC Ensembl
Innerchr3:118779280..118988000hg18UCSC Ensembl
Innerchr3:118779280..118988000hg17UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38208721
hg19208721
hg18208721
hg17208721
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522086
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694858
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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