A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618326



Internal ID21810373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44603141..44603141hg38UCSC Ensembl
chr20:43231782..43231782hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102135
Supporting Variants
Samples
Known GenesPKIG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618326
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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