A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562131



Internal ID16349540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66638290..66818166hg38UCSC Ensembl
Innerchr13:67212422..67392298hg19UCSC Ensembl
Innerchr13:66110423..66290299hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38179877
hg19179877
hg18179877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175951
SamplesNINDS_69
Known GenesPCDH9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562131
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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