A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483686



Internal ID261119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15792000..15818000hg38UCSC Ensembl
chr9:15791998..15817998hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3826001
hg1926001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021581
Samples
Known GenesCCDC171
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483686
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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