A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023252



Internal ID83223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69756771..69766543hg38UCSC Ensembl
chr9:72371687..72381459hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg389773
hg199773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478607
Supporting Variants
Samples
Known GenesPTAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023252
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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