A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489730



Internal ID267002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21284036..21306424hg38UCSC Ensembl
chr9:21284035..21306423hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3822389
hg1922389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023418
Samples
Known GenesIFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489730
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