A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5414237



Internal ID193523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53086897..53087027hg38UCSC Ensembl
chrX:53116079..53116209hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737019
Samples
Known GenesTSPYL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5414237
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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