A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563305



Internal ID16350714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113207817..113209976hg38UCSC Ensembl
Innerchr13:113862131..113864290hg19UCSC Ensembl
Innerchr13:112910132..112912291hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382160
hg192160
hg182160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820491
Samples
Known GenesCUL4A, PCID2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563305
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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