A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542569



Internal ID21866924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105902351..105902505hg38UCSC Ensembl
chr3:105621198..105621352hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990939
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542569
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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