A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933692



Internal ID23195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45121260..45121313hg38UCSC Ensembl
chr3:45162752..45162805hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447926
Supporting Variants
Samples
Known GenesCDCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933692
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