A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704357



Internal ID15441009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:76571856..76688603hg38UCSC Ensembl
Innerchr16:76605753..76722500hg19UCSC Ensembl
Innerchr16:75163254..75280001hg18UCSC Ensembl
Innerchr16:75163254..75280001hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38116748
hg19116748
hg18116748
hg17116748
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527859
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704357
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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