A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740169



Internal ID163835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54788301..54825171hg38UCSC Ensembl
chrX:54814734..54851604hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3836871
hg1936871
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537708
Supporting Variants
Samples
Known GenesITIH6, MAGED2, SNORA11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740169
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.013117


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