A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533088



Internal ID21857444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4301089..4351674hg38UCSC Ensembl
chr3:4342773..4393358hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3850586
hg1950586
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993382
Supporting Variants
Samples
Known GenesSETMAR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533088
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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