A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702733



Internal ID15439385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19639917..20009156hg38UCSC Ensembl
Innerchr21:21012231..21381470hg19UCSC Ensembl
Innerchr21:19934102..20303341hg18UCSC Ensembl
Innerchr21:19934102..20303341hg17UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38369240
hg19369240
hg18369240
hg17369240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526430
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702733
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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