A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111356



Internal ID22020590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152722562..152814788hg38UCSC Ensembl
chrX:151891051..151983320hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3892227
hg1992270
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645868
Samples
Known GenesCSAG1, CSAG2, CSAG3, CSAG4, MAGEA12, MAGEA2, MAGEA2B, MAGEA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111356
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