A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14206373



Internal ID4208189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69660111..69670995hg38UCSC Ensembl
Innerchr11:69660111..69670995hg38UCSC Ensembl
Outerchr11:69659611..69671495hg38UCSC Ensembl
chr11:69474879..69485763hg19UCSC Ensembl
Innerchr11:69474879..69485763hg19UCSC Ensembl
Outerchr11:69474379..69486263hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3810885
hg1910885
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626752
Supporting Variants
SamplesHG00186
Known GenesORAOV1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14206373
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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