A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508324



Internal ID285019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93337762..93339535hg38UCSC Ensembl
chr12:93731538..93733311hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381774
hg191774
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17684131
Samples
Known GenesLOC643339
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508324
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