A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563172



Internal ID16350581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111029653..111098935hg38UCSC Ensembl
Innerchr13:111682000..111751282hg19UCSC Ensembl
Innerchr13:110480001..110549283hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3869283
hg1969283
hg1869283
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3405n54
Supporting Variantsnssv819933
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563172
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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