A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563454



Internal ID16350863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:114139190..114158480hg38UCSC Ensembl
Innerchr13:114904665..114923955hg19UCSC Ensembl
Innerchr13:113922767..113942057hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3819291
hg1919291
hg1819291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3464n54
Supporting Variantsnssv820906, nssv820905
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563454
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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