A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14466366



Internal ID22184193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65645191..66183068hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38537878
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3554053
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14466366
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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