A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627525



Internal ID7014353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102301328..102310287hg38UCSC Ensembl
Innerchr11:102301369..102310246hg38UCSC Ensembl
Outerchr11:102301287..102310328hg38UCSC Ensembl
chr11:102172059..102181018hg19UCSC Ensembl
Innerchr11:102172100..102180977hg19UCSC Ensembl
Outerchr11:102172018..102181059hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg388960
hg198960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14253634
SamplesHG01598
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627525
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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