A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737909



Internal ID161575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149534819..149945512hg38UCSC Ensembl
chrX:148616351..149113730hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38410694
hg19497380
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557365
Supporting Variants
Samples
Known GenesCXorf40A, CXorf40B, HSFX1, HSFX2, LINC00893, LINC00894, MAGEA11, MAGEA8, MAGEA8-AS1, MAGEA9, MAGEA9B, TMEM185A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737909
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.085545


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