A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587362



Internal ID16374771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:31295691..31619348hg38UCSC Ensembl
Innerchr21:32668006..32991661hg19UCSC Ensembl
Innerchr21:31589877..31913532hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38323658
hg19323656
hg18323656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946604
Samples
Known GenesTIAM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587362
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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