A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14255562



Internal ID5580142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102878385..102882624hg38UCSC Ensembl
Innerchr11:102878385..102882624hg38UCSC Ensembl
Outerchr11:102878167..102882854hg38UCSC Ensembl
chr11:102749115..102753354hg19UCSC Ensembl
Innerchr11:102749115..102753354hg19UCSC Ensembl
Outerchr11:102748897..102753584hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg384240
hg194240
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627537
Supporting Variants
SamplesNA19024
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14255562
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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