A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3556036



Internal ID22424869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:21836222..22618492hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38782271
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14464222, nssv14454685, nssv14457717, nssv14462367, nssv14453793, nssv14459503, nssv14460130, nssv14466818
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3556036
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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