A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591724



Internal ID16379133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:131741595..131778163hg38UCSC Ensembl
Innerchr3:131460439..131497007hg19UCSC Ensembl
Innerchr3:132943129..132979697hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3836569
hg1936569
hg1836569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv973610
Samples
Known GenesCPNE4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591724
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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