A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617868



Internal ID21809915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18161464..18161464hg38UCSC Ensembl
chr19:18272274..18272274hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105129
Supporting Variants
Samples
Known GenesPIK3R2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617868
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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