A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738076



Internal ID161742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153481273..153481323hg38UCSC Ensembl
chrX:152746731..152746781hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422987
Supporting Variants
Samples
Known GenesHAUS7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738076
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.085393


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