A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527360



Internal ID303461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67382736..67383017hg38UCSC Ensembl
chr15:67675074..67675355hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702921
Samples
Known GenesIQCH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527360
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