A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3238045



Internal ID22374042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:120223481..120684157hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38460677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14463761, nssv14460041, nssv14463850, nssv14462918, nssv14464781, nssv14465648, nssv14464990, nssv14458006, nssv14464246
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3238045
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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