A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589307



Internal ID16030030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:815642..1386951hg38UCSC Ensembl
Innerchr3:857325..1428635hg19UCSC Ensembl
Innerchr3:832325..1403635hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38571310
hg19571311
hg18571311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8154n54
Supporting Variantsnssv957815
Samples
Known GenesCNTN6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589307
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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