A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17539208



Internal ID21863563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120413800..120413800hg38UCSC Ensembl
chr3:120132647..120132647hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070338
Supporting Variants
Samples
Known GenesFSTL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17539208
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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