A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628023



Internal ID7014848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127405100..127410110hg38UCSC Ensembl
Innerchr11:127405100..127410110hg38UCSC Ensembl
Outerchr11:127404853..127410300hg38UCSC Ensembl
chr11:127274995..127280005hg19UCSC Ensembl
Innerchr11:127274995..127280005hg19UCSC Ensembl
Outerchr11:127274748..127280195hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg385011
hg195011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14305147, essv14305156, essv14305149, essv14305148, essv14305144, essv14305158, essv14305151, essv14305153, essv14305159, essv14305152, essv14305154, essv14305155, essv14305146, essv14305157, essv14305145, essv14305150
SamplesHG02433, NA19190, HG02895, HG03464, HG03105, NA19189, NA19445, HG02334, NA19095, HG02772, NA19321, HG03433, HG02941, NA19467, NA19102, NA18522
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628023
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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