A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562136



Internal ID16349545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66781486..66911015hg38UCSC Ensembl
Innerchr13:67355618..67485147hg19UCSC Ensembl
Innerchr13:66253619..66383148hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38129530
hg19129530
hg18129530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813410
Samples
Known GenesPCDH9, PCDH9-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562136
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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