A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965279



Internal ID44172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40101278..40101511hg38UCSC Ensembl
chr5:40101380..40101613hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470771
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965279
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004683


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