A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5445428



Internal ID223777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167279000..167293574hg38UCSC Ensembl
chr3:166996788..167011362hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3814575
hg1914575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735002
Samples
Known GenesZBBX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5445428
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