A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562985



Internal ID16003708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103282868..103485612hg38UCSC Ensembl
Innerchr13:103935218..104137962hg19UCSC Ensembl
Innerchr13:102733219..102935963hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38202745
hg19202745
hg18202745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148927
SamplesHGDP00738
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562985
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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