A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627526



Internal ID6667673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102397022..102398271hg38UCSC Ensembl
Innerchr11:102397080..102398214hg38UCSC Ensembl
Outerchr11:102396965..102398329hg38UCSC Ensembl
chr11:102267753..102269002hg19UCSC Ensembl
Innerchr11:102267811..102268945hg19UCSC Ensembl
Outerchr11:102267696..102269060hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381250
hg191250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14253635
SamplesHG00672
Known GenesTMEM123
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627526
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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