A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483419



Internal ID260853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87401542..87402414hg38UCSC Ensembl
chr9:90016457..90017329hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38873
hg19873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025589
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483419
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