A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957987



Internal ID15905257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2526528..2622073hg38UCSC Ensembl
Innerchr3:2568212..2663757hg19UCSC Ensembl
Innerchr3:2543212..2638757hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3895546
hg1995546
hg1895546
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589389
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)nssv957987
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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