A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14252467



Internal ID6518521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102174552..102180703hg38UCSC Ensembl
Innerchr11:102174555..102180701hg38UCSC Ensembl
Outerchr11:102174550..102180706hg38UCSC Ensembl
chr11:102045283..102051434hg19UCSC Ensembl
Innerchr11:102045286..102051432hg19UCSC Ensembl
Outerchr11:102045281..102051437hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg386152
hg196152
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627522
Supporting Variants
SamplesNA20541
Known GenesYAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14252467
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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