A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284919



Internal ID20494137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34244772..34273839hg38UCSC Ensembl
chr9:34244770..34273837hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3829068
hg1929068
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754041
Supporting Variants
Samples
Known GenesKIF24, UBAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284919
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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