A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449941



Internal ID228161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26626776..26626906hg38UCSC Ensembl
chr3:26668267..26668397hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932068
Samples
Known GenesLRRC3B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449941
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