A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485196



Internal ID262592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15461354..15461413hg38UCSC Ensembl
chr9:15461352..15461411hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020608
Samples
Known GenesSNAPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485196
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