A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1239n223



Internal ID22804207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82139001..82192600hg38UCSC Ensembl
chr11:81850043..81903642hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3853600
hg1953600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6456808, nsv6470757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1239n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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