A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561202



Internal ID16348611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19157877..19184771hg38UCSC Ensembl
Innerchr13:19732017..19758911hg19UCSC Ensembl
Innerchr13:18630017..18656911hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3826895
hg1926895
hg1826895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175913
Samples1780862081_A
Known GenesTUBA3C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561202
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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