A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519906



Internal ID296247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66266555..66270912hg38UCSC Ensembl
chr15:66558893..66563250hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384358
hg194358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704325
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519906
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