A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561308



Internal ID334291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48157791..48277732hg38UCSC Ensembl
chrX:48017219..48137167hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38119942
hg19119949
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736829
Samples
Known GenesSSX1, SSX5
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561308
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer