A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936483



Internal ID25048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115326840..115327218hg38UCSC Ensembl
chr3:115045687..115046065hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444343
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936483
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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