A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587334



Internal ID16374743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:26263596..26478652hg38UCSC Ensembl
Innerchr21:27635915..27850971hg19UCSC Ensembl
Innerchr21:26557786..26772842hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38215057
hg19215057
hg18215057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946585
Samples
Known GenesCYYR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587334
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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