A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946606



Internal ID15893876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:31820819..31932178hg38UCSC Ensembl
Innerchr21:33193131..33304490hg19UCSC Ensembl
Innerchr21:32115002..32226361hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38111360
hg19111360
hg18111360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587365
Supporting Variants
Samples
Known GenesHUNK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946606
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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