A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737019



Internal ID160685
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 StatusS
Merged Variantsnsv5414237
Supporting Variants
Samples
Known GenesTSPYL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737019
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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