A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626619



Internal ID7013451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63038399..63058408hg38UCSC Ensembl
Innerchr11:63038399..63058408hg38UCSC Ensembl
Outerchr11:63037899..63058908hg38UCSC Ensembl
chr11:62805871..62825880hg19UCSC Ensembl
Innerchr11:62805871..62825880hg19UCSC Ensembl
Outerchr11:62805371..62826380hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3820010
hg1920010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14182102, essv14182101
SamplesHG03385, NA18522
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626619
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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