A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562926



Internal ID16350335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98654144..98669118hg38UCSC Ensembl
Innerchr13:99306398..99321372hg19UCSC Ensembl
Innerchr13:98104399..98119373hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3814975
hg1914975
hg1814975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv818083
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562926
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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