A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628147



Internal ID6668291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133287960..133291470hg38UCSC Ensembl
Innerchr11:133287960..133291470hg38UCSC Ensembl
Outerchr11:133287748..133291686hg38UCSC Ensembl
chr11:133157855..133161365hg19UCSC Ensembl
Innerchr11:133157855..133161365hg19UCSC Ensembl
Outerchr11:133157643..133161581hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383511
hg193511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14318219
SamplesNA19834
Known GenesOPCML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628147
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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