A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14040182



Internal ID5072982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18052738..18054615hg38UCSC Ensembl
Innerchr11:18052751..18054603hg38UCSC Ensembl
Outerchr11:18052726..18054628hg38UCSC Ensembl
chr11:18074285..18076162hg19UCSC Ensembl
Innerchr11:18074298..18076150hg19UCSC Ensembl
Outerchr11:18074273..18076175hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381878
hg191878
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625485
Supporting Variants
SamplesNA18541
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14040182
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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