A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562771



Internal ID16350180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95290238..95375253hg38UCSC Ensembl
Innerchr13:95942492..96027507hg19UCSC Ensembl
Innerchr13:94740493..94825508hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3885016
hg1985016
hg1885016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3327n54
Supporting Variantsnssv817539, nssv817537, nssv817538
Samples
Known GenesABCC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562771
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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