A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742151



Internal ID165817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115839475..115888475hg38UCSC Ensembl
chrX:114955808..115004808hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3849001
hg1949001
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421687
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742151
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.499779


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