A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627723



Internal ID7014551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110828665..110833247hg38UCSC Ensembl
Innerchr11:110828665..110833247hg38UCSC Ensembl
Outerchr11:110828528..110833355hg38UCSC Ensembl
chr11:110699388..110703970hg19UCSC Ensembl
Innerchr11:110699388..110703970hg19UCSC Ensembl
Outerchr11:110699251..110704078hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg384583
hg194583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14286810
SamplesNA19064
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627723
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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