A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5445231



Internal ID223587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160326312..160326475hg38UCSC Ensembl
chr3:160044100..160044263hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940173
Samples
Known GenesIFT80
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5445231
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