A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667562



Internal ID9586981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64318057..64320053hg38UCSC Ensembl
Outerchr11:64317900..64320206hg38UCSC Ensembl
Innerchr11:64085529..64087525hg19UCSC Ensembl
Outerchr11:64085372..64087678hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382307
hg192307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5584113
SamplesNA18907
Known GenesPRDX5, TRMT112
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667562
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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