A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626388



Internal ID21818435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17659134..17659134hg38UCSC Ensembl
chr20:17639779..17639779hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106565
Supporting Variants
Samples
Known GenesRRBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626388
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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