A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv168n206



Internal ID22755472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37318550..37322218hg38UCSC Ensembl
chr15:37610751..37614419hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg383669
hg193669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5512319, nsv5510042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv168n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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