A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3551671



Internal ID22420577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153066014..153084051hg38UCSC Ensembl
chrX:152234380..152349904hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3818038
hg19115525
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14454894, nssv14465136, nssv14453181
SamplesNA19240, HG00733, HG00514
Known GenesPNMA6A, PNMA6C
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3551671
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer