A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562130



Internal ID16349539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66626522..66732651hg38UCSC Ensembl
Innerchr13:67200654..67306783hg19UCSC Ensembl
Innerchr13:66098655..66204784hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38106130
hg19106130
hg18106130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813408
Samples
Known GenesPCDH9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562130
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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