A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587185



Internal ID16374594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19639917..19994393hg38UCSC Ensembl
Innerchr21:21012231..21366707hg19UCSC Ensembl
Innerchr21:19934102..20288578hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38354477
hg19354477
hg18354477
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946236
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587185
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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