A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17440198



Internal ID22498068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153075458..153180072hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38104615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868579
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17440198
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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