A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105096



Internal ID22014329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152719451..153060710hg38UCSC Ensembl
chrX:151887940..152229070hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38341260
hg19341131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638403
Samples
Known GenesCETN2, CSAG1, CSAG2, CSAG3, CSAG4, MAGEA12, MAGEA2, MAGEA2B, MAGEA3, NSDHL, PNMA3, PNMA5, ZNF185
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105096
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