A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626659



Internal ID6666809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64317918..64320057hg38UCSC Ensembl
Innerchr11:64317937..64320038hg38UCSC Ensembl
Outerchr11:64317899..64320076hg38UCSC Ensembl
chr11:64085390..64087529hg19UCSC Ensembl
Innerchr11:64085409..64087510hg19UCSC Ensembl
Outerchr11:64085371..64087548hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382140
hg192140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14184928
SamplesNA18907
Known GenesPRDX5, TRMT112
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626659
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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