A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992920



Internal ID21902263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192219545..192270858hg38UCSC Ensembl
chr3:191937334..191988647hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3851314
hg1951314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540957
Samples
Known GenesFGF12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992920
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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