A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478123



Internal ID255688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102985453..102991782hg38UCSC Ensembl
chr8:103997681..104004010hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg386330
hg196330
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015831
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478123
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