A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281351



Internal ID20490569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149573866..149795524hg38UCSC Ensembl
chrX:148655522..148877186hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38221659
hg19221665
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752636
Supporting Variants
Samples
Known GenesHSFX1, HSFX2, MAGEA11, MAGEA9, MAGEA9B, TMEM185A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281351
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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