A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589374



Internal ID16030097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2301356..2315374hg38UCSC Ensembl
Innerchr3:2343040..2357058hg19UCSC Ensembl
Innerchr3:2318040..2332058hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3814019
hg1914019
hg1814019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152441
SamplesNINDS_91
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589374
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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