A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260747



Internal ID20469965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72996084..73086935hg38UCSC Ensembl
chrX:72215923..72306774hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3890852
hg1990852
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757377
Supporting Variants
Samples
Known GenesPABPC1L2A, PABPC1L2B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260747
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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