A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940132



Internal ID27467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158785543..158785594hg38UCSC Ensembl
chr3:158503332..158503383hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940132
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.020013


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