A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738054



Internal ID161720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153095878..153095977hg38UCSC Ensembl
chrX:152361706..152361805hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738054
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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