A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627520



Internal ID7014348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102022365..102025891hg38UCSC Ensembl
Innerchr11:102022373..102025884hg38UCSC Ensembl
Outerchr11:102022358..102025899hg38UCSC Ensembl
chr11:101893096..101896622hg19UCSC Ensembl
Innerchr11:101893104..101896615hg19UCSC Ensembl
Outerchr11:101893089..101896630hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg383527
hg193527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14252457
SamplesHG01628
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627520
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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