A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627755



Internal ID7014583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112393016..112396620hg38UCSC Ensembl
Innerchr11:112393066..112396570hg38UCSC Ensembl
Outerchr11:112392966..112396670hg38UCSC Ensembl
chr11:112263739..112267343hg19UCSC Ensembl
Innerchr11:112263789..112267293hg19UCSC Ensembl
Outerchr11:112263689..112267393hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg383605
hg193605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14287905, essv14287908, essv14287907, essv14287906
SamplesHG00640, HG01702, HG01705, NA20763
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627755
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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