A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553180



Internal ID21877535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133884997..133884997hg38UCSC Ensembl
chr3:133603841..133603841hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067041
Supporting Variants
Samples
Known GenesRAB6B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553180
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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