A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14295781



Internal ID6441563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122229664..122236100hg38UCSC Ensembl
Innerchr11:122229664..122236100hg38UCSC Ensembl
Outerchr11:122229164..122236600hg38UCSC Ensembl
chr11:122100372..122106808hg19UCSC Ensembl
Innerchr11:122100372..122106808hg19UCSC Ensembl
Outerchr11:122099872..122107308hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg386437
hg196437
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627939
Supporting Variants
SamplesNA20509
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14295781
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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