A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14454898



Internal ID22269076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:144077028..144882807hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38805780
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3547267
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14454898
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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