A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14292581



Internal ID3139660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117102937..117114821hg38UCSC Ensembl
Innerchr11:117103437..117114321hg38UCSC Ensembl
Outerchr11:117101937..117115821hg38UCSC Ensembl
chr11:116973653..116985537hg19UCSC Ensembl
Innerchr11:116974153..116985037hg19UCSC Ensembl
Outerchr11:116972653..116986537hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3811885
hg1911885
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627844
Supporting Variants
SamplesHG02768
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14292581
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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