A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421674



Internal ID22479544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33393119..33463866hg38UCSC Ensembl
chr5:33393225..33463971hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3870748
hg1970747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889778
Supporting Variants
Samples
Known GenesTARS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421674
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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