A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628051



Internal ID6668195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128890799..128892879hg38UCSC Ensembl
Innerchr11:128890824..128892854hg38UCSC Ensembl
Outerchr11:128890774..128892904hg38UCSC Ensembl
chr11:128760694..128762774hg19UCSC Ensembl
Innerchr11:128760719..128762749hg19UCSC Ensembl
Outerchr11:128760669..128762799hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382081
hg192081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14308937, essv14308938
SamplesNA20814, NA18963
Known GenesKCNJ5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628051
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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