A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697503



Internal ID15434155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:16685314..16693888hg38UCSC Ensembl
Innerchr21:18057633..18066207hg19UCSC Ensembl
Innerchr21:16979504..16988078hg18UCSC Ensembl
Innerchr21:16979504..16988078hg17UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg388575
hg198575
hg188575
hg178575
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520583
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697503
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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