A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626928



Internal ID7013758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80060975..80107725hg38UCSC Ensembl
Innerchr11:80060985..80107716hg38UCSC Ensembl
Outerchr11:80060966..80107735hg38UCSC Ensembl
chr11:79772018..79818769hg19UCSC Ensembl
Innerchr11:79772028..79818760hg19UCSC Ensembl
Outerchr11:79772009..79818779hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3846751
hg1946752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14216136, essv14216133, essv14216135, essv14216134
SamplesHG03717, HG03786, HG03900, HG03611
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626928
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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