A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14295723



Internal ID5707022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122058955..122061198hg38UCSC Ensembl
Innerchr11:122059011..122061143hg38UCSC Ensembl
Outerchr11:122058900..122061254hg38UCSC Ensembl
chr11:121929663..121931906hg19UCSC Ensembl
Innerchr11:121929719..121931851hg19UCSC Ensembl
Outerchr11:121929608..121931962hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382244
hg192244
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627936
Supporting Variants
SamplesNA19091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14295723
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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