A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656616



Internal ID9576035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128890840..128892890hg38UCSC Ensembl
Outerchr11:128890803..128892940hg38UCSC Ensembl
Innerchr11:128760735..128762785hg19UCSC Ensembl
Outerchr11:128760698..128762835hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382138
hg192138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5911575
SamplesNA20814
Known GenesKCNJ5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656616
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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