A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16963075



Internal ID42713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28325025..28334910hg38UCSC Ensembl
chr5:28325132..28335017hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg389886
hg199886
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465903
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16963075
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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