A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561669



Internal ID16349078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:52846209..52848970hg38UCSC Ensembl
Innerchr13:53420344..53423105hg19UCSC Ensembl
Innerchr13:52318345..52321106hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg382762
hg192762
hg182762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv811708
Samples
Known GenesPCDH8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561669
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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