A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259781



Internal ID20468999
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 StatusS
Merged Variantsnsv4751211
Supporting Variants
Samples
Known GenesFAIM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259781
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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