A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509124



Internal ID285789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90499921..90512216hg38UCSC Ensembl
chr12:90893698..90905993hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3812296
hg1912296
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17689944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509124
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