A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666169



Internal ID9932274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:110828712..110833147hg38UCSC Ensembl
Outerchr11:110828675..110833197hg38UCSC Ensembl
Innerchr11:110699435..110703870hg19UCSC Ensembl
Outerchr11:110699398..110703920hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg384523
hg194523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5846536
SamplesNA19064
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666169
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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