A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv809837



Internal ID15757107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:40940324..41070586hg38UCSC Ensembl
Innerchr13:41514460..41644722hg19UCSC Ensembl
Innerchr13:40412460..40542722hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38130263
hg19130263
hg18130263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561538
Supporting Variants
Samples
Known GenesELF1, WBP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv809837
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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