A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111402



Internal ID22020636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149650096..149819485hg38UCSC Ensembl
chrX:148731765..148901147hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38169390
hg19169383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637713
Samples
Known GenesHSFX1, HSFX2, MAGEA11, MAGEA9, MAGEA9B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111402
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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