A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16942799



Internal ID29203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171104973..171105032hg38UCSC Ensembl
chr3:170822762..170822821hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439222
Supporting Variants
Samples
Known GenesTNIK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16942799
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.012644


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