A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936375



Internal ID24977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112086060..112086162hg38UCSC Ensembl
chr3:111804907..111805009hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446547
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936375
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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