A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv289n209



Internal ID22826364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116810117..116814324hg38UCSC Ensembl
chr11:116680833..116685040hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg384208
hg194208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5927427, nsv5915622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv289n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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