A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14459767



Internal ID22269435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18215202..18357590hg38UCSC Ensembl
chrUn_gl000212:43954..186342hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38142389
hg19142389
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3551642
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14459767
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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