A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957980



Internal ID15905250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2454047..2454809hg38UCSC Ensembl
Innerchr3:2495731..2496493hg19UCSC Ensembl
Innerchr3:2470731..2471493hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38763
hg19763
hg18763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589384
Supporting Variants
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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