A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520583



Internal ID15447876
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697503
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520583
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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