A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586972



Internal ID16027695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10324453..10651108hg38UCSC Ensembl
Innerchr21:10861349..11188004hg19UCSC Ensembl
Innerchr21:9883220..10209875hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38326656
hg19326656
hg18326656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7743n54
Supporting Variantsnssv944864
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586972
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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