A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14458122



Internal ID22252047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42612724..42672932hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3860209
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3556495
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14458122
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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