A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940676



Internal ID27823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141993309..141993382hg38UCSC Ensembl
chr3:141712151..141712224hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437139
Supporting Variants
Samples
Known GenesTFDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940676
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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