A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587366



Internal ID16374775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:32054573..32095347hg38UCSC Ensembl
Innerchr21:33426886..33467660hg19UCSC Ensembl
Innerchr21:32348757..32389531hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3840775
hg1940775
hg1840775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946607
Samples
Known GenesLINC00159
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587366
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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