A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589373



Internal ID16030096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2267695..2773579hg38UCSC Ensembl
Innerchr3:2309379..2815263hg19UCSC Ensembl
Innerchr3:2284379..2790263hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38505885
hg19505885
hg18505885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8166n54
Supporting Variantsnssv1152440
SamplesHGDP01396
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589373
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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