A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14184860



Internal ID5648039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63672505..63677266hg38UCSC Ensembl
Innerchr11:63672505..63677266hg38UCSC Ensembl
Outerchr11:63672236..63677528hg38UCSC Ensembl
chr11:63439977..63444738hg19UCSC Ensembl
Innerchr11:63439977..63444738hg19UCSC Ensembl
Outerchr11:63439708..63445000hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384762
hg194762
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626648
Supporting Variants
SamplesNA19065
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14184860
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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