A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520325



Internal ID296656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88308992..88309323hg38UCSC Ensembl
chr16:88342598..88342929hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17710525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520325
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