A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563723



Internal ID336653
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 StatusM
Merged Variants
Supporting Variantsnssv17742360
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563723
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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