A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939805



Internal ID27256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128574628..128574993hg38UCSC Ensembl
chr3:128293471..128293836hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435642
Supporting Variants
Samples
Known GenesC3orf27
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939805
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002812


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