A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533817



Internal ID309695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73807205..73807274hg38UCSC Ensembl
chr15:74099546..74099615hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533817
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