A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737924



Internal ID161590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149778100..149918000hg38UCSC Ensembl
chrX:148859762..149086218hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38139901
hg19226457
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415282
Supporting Variants
Samples
Known GenesMAGEA8, MAGEA8-AS1, MAGEA9, MAGEA9B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737924
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0233993


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