A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671741



Internal ID9937846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77519180..77521834hg38UCSC Ensembl
chr11:77230225..77232879hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382655
hg192655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6366443, essv5664123
SamplesNA20811, NA20786
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671741
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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