A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532137



Internal ID308066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45999707..46212161hg38UCSC Ensembl
chr15:46291905..46504359hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38212455
hg19212455
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532137
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