A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2113n54



Internal ID22770008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:98695864..98819928hg38UCSC Ensembl
chr11:98566594..98690658hg19UCSC Ensembl
chr11:98071804..98195868hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38124065
hg19124065
hg18124065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556038, nsv556039
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2113n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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