A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587274



Internal ID16374683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:23004316..23110971hg38UCSC Ensembl
Innerchr21:24376638..24483293hg19UCSC Ensembl
Innerchr21:23298509..23405164hg18UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg38106656
hg19106656
hg18106656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946501
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587274
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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