A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14463742



Internal ID22276895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10806629..10809752hg38UCSC Ensembl
chr20:10787277..10790400hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg383124
hg193124
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3236455
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14463742
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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