A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967532



Internal ID45669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72902608..72906549hg38UCSC Ensembl
chr5:72198435..72202376hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg383942
hg193942
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561904
Supporting Variants
Samples
Known GenesTNPO1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967532
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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