A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486038



Internal ID263414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21227652..21239414hg38UCSC Ensembl
chr9:21227651..21239413hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3811763
hg1911763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022484
Samples
Known GenesIFNA14, IFNA17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486038
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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