A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962155



Internal ID42068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17092073..17098237hg38UCSC Ensembl
chr5:17092182..17098346hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg386165
hg196165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140842
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962155
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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