A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559419



Internal ID332452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48359523..48446869hg38UCSC Ensembl
chrX:48218958..48305249hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3887347
hg1986292
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736845
Samples
Known GenesSSX4, SSX4B
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559419
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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