A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960300



Internal ID22735285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39029440..39049501hg38UCSC Ensembl
chr22:39425445..39445506hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3820062
hg1920062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391189
Samples
Known GenesAPOBEC3D, APOBEC3F
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960300
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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