A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293174



Internal ID20502392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154589692..154614731hg38UCSC Ensembl
chrX:153817952..153842987hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3825040
hg1925036
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754521
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293174
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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