A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938396



Internal ID26328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115698065..115698123hg38UCSC Ensembl
chr3:115416912..115416970hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449627
Supporting Variants
Samples
Known GenesGAP43
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938396
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002654


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