A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079231



Internal ID21988464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180920683..180920683hg38UCSC Ensembl
chr3:180638471..180638471hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546879
Samples
Known GenesFXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079231
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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