A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666877



Internal ID21615184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72996081..73087487hg38UCSC Ensembl
chrX:72215920..72307326hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3891407
hg1991407
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168279
Samples
Known GenesPABPC1L2A, PABPC1L2B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666877
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer