A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484883



Internal ID262285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94848319..94848467hg38UCSC Ensembl
chr9:97610601..97610749hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025817
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484883
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