A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv811699



Internal ID16105655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:52846209..52847078hg38UCSC Ensembl
Innerchr13:53420344..53421213hg19UCSC Ensembl
Innerchr13:52318345..52319214hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38870
hg19870
hg18870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561663
Supporting Variants
Samples
Known GenesPCDH8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv811699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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