A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626752



Internal ID6666900
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14206374, essv14206372, essv14206373
SamplesHG00182, NA12272, HG00186
Known GenesORAOV1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626752
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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