A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944314



Internal ID30212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196846474..196846751hg38UCSC Ensembl
chr3:196573345..196573622hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446183
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944314
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