A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509370



Internal ID286024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22586900..22704242hg38UCSC Ensembl
chr15:23168854..23286196hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38117343
hg19117343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698523
Samples
Known GenesGOLGA8I, HERC2P2, WHAMMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509370
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