A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14464263



Internal ID22261718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41768334..42093866hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38325533
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3545212
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14464263
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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