A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742139



Internal ID165805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115565342..115567043hg38UCSC Ensembl
chrX:114799668..114801365hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg381702
hg191698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427331
Supporting Variants
Samples
Known GenesPLS3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742139
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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