A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736826



Internal ID160492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48141837..48427837hg38UCSC Ensembl
chrX:48001265..48286224hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38286001
hg19284960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421437
Supporting Variants
Samples
Known GenesSSX1, SSX3, SSX4, SSX4B, SSX5, SSX9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736826
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000841928


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