A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627892



Internal ID7014717
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14293356, essv14293358, essv14293359, essv14293357
SamplesNA19107, NA19197, HG02051, NA18488
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627892
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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