A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940386



Internal ID27639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143175172..143243042hg38UCSC Ensembl
chr3:142894014..142961884hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3867871
hg1967871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445878
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940386
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer