A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929498



Internal ID20394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13182000..13206000hg38UCSC Ensembl
chr3:13223500..13247500hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3824001
hg1924001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139162
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929498
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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