A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146696



Internal ID345901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:12634335..12657000hg38UCSC Ensembl
chr20:12614982..12637647hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3822666
hg1922666
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146696
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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