A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627537



Internal ID7014365
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14255556, essv14255561, essv14255557, essv14255552, essv14255559, essv14255554, essv14255563, essv14255550, essv14255553, essv14255558, essv14255551, essv14255560, essv14255555, essv14255562
SamplesHG00442, HG02337, HG03455, HG03133, HG03479, NA20278, NA19024, HG03054, HG03575, NA18910, HG03294, HG02611, HG02107, HG03162
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627537
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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