A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421437



Internal ID200508
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 StatusM
Merged Variants
Supporting Variantsnssv17736826
Samples
Known GenesSSX1, SSX3, SSX4, SSX4B, SSX5, SSX9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421437
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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