A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14465955



Internal ID22198917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69727516..69728993hg38UCSC Ensembl
chr16:69761419..69762896hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381478
hg191478
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3236928
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14465955
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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