A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489026



Internal ID266319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111947710..111948891hg38UCSC Ensembl
chr9:114709990..114711171hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381182
hg191182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489026
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