A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562768



Internal ID16350177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95197563..95206432hg38UCSC Ensembl
Innerchr13:95849817..95858686hg19UCSC Ensembl
Innerchr13:94647818..94656687hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg388870
hg198870
hg188870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817535
Samples
Known GenesABCC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562768
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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