A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658774



Internal ID9924879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:105542622..105545807hg38UCSC Ensembl
Outerchr11:105542585..105545857hg38UCSC Ensembl
Innerchr11:105413349..105416534hg19UCSC Ensembl
Outerchr11:105413312..105416584hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383273
hg193273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5421855
SamplesNA18502
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658774
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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