A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751211



Internal ID20527071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138609555..138609555hg38UCSC Ensembl
chr3:138328397..138328397hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259781
Samples
Known GenesFAIM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751211
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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