A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742025



Internal ID165691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112574542..112597300hg38UCSC Ensembl
chrX:111817770..111840528hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3822759
hg1922759
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138438
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742025
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000418498


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