A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623076



Internal ID21815123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1259604..1259604hg38UCSC Ensembl
chr20:1240248..1240248hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109557
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623076
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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