A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626945



Internal ID7013775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81160403..81168557hg38UCSC Ensembl
Innerchr11:81160903..81168057hg38UCSC Ensembl
Outerchr11:81159403..81169557hg38UCSC Ensembl
chr11:80871446..80879600hg19UCSC Ensembl
Innerchr11:80871946..80879100hg19UCSC Ensembl
Outerchr11:80870446..80880600hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg388155
hg198155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14216404, essv14216403, essv14216407, essv14216406, essv14216405
SamplesNA19201, HG02307, HG02861, HG02643, HG03265
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626945
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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