A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106214



Internal ID22015447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73005560..73086945hg38UCSC Ensembl
chrX:72225399..72306784hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3881386
hg1981386
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643247
Samples
Known GenesPABPC1L2A, PABPC1L2B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106214
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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