A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14253634



Internal ID1719382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102301328..102310287hg38UCSC Ensembl
Innerchr11:102301369..102310246hg38UCSC Ensembl
Outerchr11:102301287..102310328hg38UCSC Ensembl
chr11:102172059..102181018hg19UCSC Ensembl
Innerchr11:102172100..102180977hg19UCSC Ensembl
Outerchr11:102172018..102181059hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg388960
hg198960
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627525
Supporting Variants
SamplesHG01598
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14253634
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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