A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv818882



Internal ID16112838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105580809..105651875hg38UCSC Ensembl
Innerchr13:106233158..106304224hg19UCSC Ensembl
Innerchr13:105031159..105102225hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3871067
hg1971067
hg1871067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563008
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv818882
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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