A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944293



Internal ID30196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196675435..196689425hg38UCSC Ensembl
chr3:196402306..196416296hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3813991
hg1913991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452971
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944293
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