A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965022



Internal ID43987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17466000..17525000hg38UCSC Ensembl
chr5:17466109..17525109hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3859001
hg1959001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965022
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002342


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