A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587471



Internal ID16374880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36964896..37000429hg38UCSC Ensembl
Innerchr21:38337196..38372729hg19UCSC Ensembl
Innerchr21:37259066..37294599hg18UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3835534
hg1935534
hg1835534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv946767
Samples
Known GenesHLCS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587471
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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