A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14216406



Internal ID3663737
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626945
Supporting Variants
SamplesHG03265
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14216406
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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