A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562137



Internal ID16349546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66818166..66863184hg38UCSC Ensembl
Innerchr13:67392298..67437316hg19UCSC Ensembl
Innerchr13:66290299..66335317hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3845019
hg1945019
hg1845019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175955
SamplesHGDP00846
Known GenesPCDH9, PCDH9-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562137
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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