A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674926



Internal ID9941031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63672491..63677244hg38UCSC Ensembl
Outerchr11:63672454..63677294hg38UCSC Ensembl
Innerchr11:63439963..63444716hg19UCSC Ensembl
Outerchr11:63439926..63444766hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384841
hg194841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6041315
SamplesNA19065
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674926
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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