A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481467



Internal ID258946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81859963..81868741hg38UCSC Ensembl
chr9:84474878..84483656hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg388779
hg198779
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026018
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481467
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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