A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3554054



Internal ID22422923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23252404..23312907hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3860504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14460340, nssv14464930, nssv14459768, nssv14457992, nssv14463103, nssv14467281, nssv14457663, nssv14461169, nssv14456453
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)nsv3554054
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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