A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096326



Internal ID21512733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1226689..1255753hg38UCSC Ensembl
chr16:1276689..1305754hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3829065
hg1929066
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670151
Supporting Variants
Samples
Known GenesTPSAB1, TPSB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096326
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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