A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742360



Internal ID166026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132176454..132176710hg38UCSC Ensembl
chrX:131310482..131310738hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563723
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742360
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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