A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14216400



Internal ID3979525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81127227..81128322hg38UCSC Ensembl
Innerchr11:81127248..81128302hg38UCSC Ensembl
Outerchr11:81127207..81128343hg38UCSC Ensembl
chr11:80838270..80839365hg19UCSC Ensembl
Innerchr11:80838291..80839345hg19UCSC Ensembl
Outerchr11:80838250..80839386hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381096
hg191096
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626944
Supporting Variants
SamplesHG03634
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14216400
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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