A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591639



Internal ID16379048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128702323..128713872hg38UCSC Ensembl
Innerchr3:128421166..128432715hg19UCSC Ensembl
Innerchr3:129903856..129915405hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3811550
hg1911550
hg1811550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv973054
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591639
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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