A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481115



Internal ID258610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90132691..90165271hg38UCSC Ensembl
chr8:91144919..91177499hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3832581
hg1932581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013532
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481115
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