A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700926



Internal ID15437578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86057292..86058024hg38UCSC Ensembl
Innerchr16:86090898..86091630hg19UCSC Ensembl
Innerchr16:84648399..84649131hg18UCSC Ensembl
Innerchr16:84648399..84649131hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38733
hg19733
hg18733
hg17733
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524914
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700926
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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