A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551117



Internal ID21875472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134211467..134211467hg38UCSC Ensembl
chr3:133930311..133930311hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6062861
Supporting Variants
Samples
Known GenesRYK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551117
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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