A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023071



Internal ID83091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62834950..62896832hg38UCSC Ensembl
chr9:66490774..66552656hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3861883
hg1961883
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430793
Supporting Variants
Samples
Known GenesPTGER4P2-CDK2AP2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023071
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.499844


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer