A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929288



Internal ID20239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4084855..4203809hg38UCSC Ensembl
chr3:4126539..4245493hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38118955
hg19118955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441944
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929288
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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