A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515297



Internal ID291780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63492245..63581768hg38UCSC Ensembl
chr16:63526149..63615672hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3889524
hg1989524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17710050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515297
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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