A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738023



Internal ID161689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152360704..152360762hg38UCSC Ensembl
chrX:151529176..151529234hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422061
Supporting Variants
Samples
Known GenesGABRA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738023
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003132


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