A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680668



Internal ID15417320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13264031..13270398hg38UCSC Ensembl
Innerchr16:13357888..13364255hg19UCSC Ensembl
Innerchr16:13265389..13271756hg18UCSC Ensembl
Innerchr16:13265389..13271756hg17UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg386368
hg196368
hg186368
hg176368
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521045
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680668
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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