A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587566



Internal ID16028289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41863326..41894948hg38UCSC Ensembl
Innerchr21:43283435..43315057hg19UCSC Ensembl
Innerchr21:42156504..42188126hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3831623
hg1931623
hg1831623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7849n54
Supporting Variantsnssv947145
Samples
Known GenesC2CD2, PRDM15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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