A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563450



Internal ID16350859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:114138947..114156293hg38UCSC Ensembl
Innerchr13:114904422..114921768hg19UCSC Ensembl
Innerchr13:113922524..113939870hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3817347
hg1917347
hg1817347
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3464n54
Supporting Variantsnssv820901
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563450
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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