A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561661



Internal ID16349070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:52845004..52891992hg38UCSC Ensembl
Innerchr13:53419139..53466127hg19UCSC Ensembl
Innerchr13:52317140..52364128hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3846989
hg1946989
hg1846989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176350
SamplesHGDP00682
Known GenesPCDH8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561661
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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