A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562098



Internal ID16349507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66524243..66576628hg38UCSC Ensembl
Innerchr13:67098375..67150760hg19UCSC Ensembl
Innerchr13:65996376..66048761hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3852386
hg1952386
hg1852386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3219n54
Supporting Variantsnssv1175946
SamplesHGDP00736
Known GenesPCDH9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562098
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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