A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562132



Internal ID16349541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66646671..66682147hg38UCSC Ensembl
Innerchr13:67220803..67256279hg19UCSC Ensembl
Innerchr13:66118804..66154280hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3835477
hg1935477
hg1835477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175952
SamplesHGDP00029
Known GenesPCDH9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562132
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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