A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966660



Internal ID45092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67339474..67339624hg38UCSC Ensembl
chr5:66635302..66635452hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141086
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966660
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005941


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