A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589314



Internal ID16030037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1037340..1101740hg38UCSC Ensembl
Innerchr3:1079024..1143424hg19UCSC Ensembl
Innerchr3:1054024..1118424hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3864401
hg1964401
hg1864401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957822
Samples
Known GenesCNTN6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589314
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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