A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14293359



Internal ID5817203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119609676..119610336hg38UCSC Ensembl
Innerchr11:119609699..119610313hg38UCSC Ensembl
Outerchr11:119609653..119610359hg38UCSC Ensembl
chr11:119480388..119481048hg19UCSC Ensembl
Innerchr11:119480411..119481025hg19UCSC Ensembl
Outerchr11:119480365..119481071hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627892
Supporting Variants
SamplesNA19197
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14293359
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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