A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659679



Internal ID9925784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17267568..17274646hg38UCSC Ensembl
Outerchr11:17267531..17274696hg38UCSC Ensembl
Innerchr11:17289115..17296193hg19UCSC Ensembl
Outerchr11:17289078..17296243hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387166
hg197166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6114382
SamplesNA19077
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659679
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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