A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488317



Internal ID265634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73318744..73321302hg38UCSC Ensembl
chr9:75933660..75936218hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382559
hg192559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022590
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488317
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer