A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv753n209



Internal ID22826828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59524092..59550463hg38UCSC Ensembl
chr15:59816291..59842662hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3826372
hg1926372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5940267, nsv5936708
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv753n209
Frequency
Sample Size914
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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