A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932725



Internal ID22708028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3653625..3669650hg38UCSC Ensembl
chr16:3703626..3719651hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3816026
hg1916026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv787n209
Supporting Variantsnssv17385315
Samples
Known GenesDNASE1, TRAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932725
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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