A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589322



Internal ID16030045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1165012..2306437hg38UCSC Ensembl
Innerchr3:1206696..2348121hg19UCSC Ensembl
Innerchr3:1181696..2323121hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381141426
hg191141426
hg181141426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957826
Samples
Known GenesCNTN4, CNTN4-AS2, CNTN6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589322
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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