A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14459110



Internal ID22143745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105053366..105056276hg38UCSC Ensembl
chr9:107815647..107818557hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382911
hg192911
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3554442
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14459110
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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