A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166274



Internal ID21430038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153074420..153084561hg38UCSC Ensembl
chrX:152242803..152350414hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3810142
hg19107612
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666401
Supporting Variants
SamplesHG00731
Known GenesPNMA6A, PNMA6C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166274
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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