A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14465264



Internal ID22130366
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
SamplesHG00513
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14465264
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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