A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625472



Internal ID7012306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17267549..17274665hg38UCSC Ensembl
Innerchr11:17267606..17274608hg38UCSC Ensembl
Outerchr11:17267492..17274722hg38UCSC Ensembl
chr11:17289096..17296212hg19UCSC Ensembl
Innerchr11:17289153..17296155hg19UCSC Ensembl
Outerchr11:17289039..17296269hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387117
hg197117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14040149
SamplesNA19077
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625472
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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