A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586902



Internal ID16027625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10324453..10772189hg38UCSC Ensembl
Innerchr21:10740268..11188004hg19UCSC Ensembl
Innerchr21:9762139..10209875hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38447737
hg19447737
hg18447737
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7729n54
Supporting Variantsnssv944791
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)nsv586902
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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