A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939116



Internal ID26794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128944223..128946294hg38UCSC Ensembl
chr3:128663066..128665137hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg382072
hg192072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450672
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939116
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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