A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760563



Internal ID20536423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73005560..73077479hg38UCSC Ensembl
chrX:72225399..72297318hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3871920
hg1971920
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv79n199
Supporting Variantsnssv16270782
Samples
Known GenesPABPC1L2A, PABPC1L2B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760563
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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