A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483865



Internal ID261292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114936661..114937256hg38UCSC Ensembl
chr9:117698941..117699536hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027793
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483865
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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