A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587541



Internal ID16374950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41510076..41638240hg38UCSC Ensembl
Innerchr21:42882003..43058400hg19UCSC Ensembl
Innerchr21:41803873..41931469hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38128165
hg19176398
hg18127597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv947040
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587541
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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