A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553838



Internal ID21878193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129530533..129530533hg38UCSC Ensembl
chr3:129249376..129249376hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065913
Supporting Variants
Samples
Known GenesRHO
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553838
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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