A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14454894



Internal ID22183306
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3551671
Supporting Variants
SamplesHG00514
Known GenesPNMA6A, PNMA6C
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14454894
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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