A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14286810



Internal ID5643955
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627723
Supporting Variants
SamplesNA19064
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14286810
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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