A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3236912



Internal ID22373732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152705955..152752524hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3846570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14459948, nssv14463243, nssv14455549, nssv14459316, nssv14454089
SamplesNA19238, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3236912
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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