A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362401



Internal ID21019954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:166095030..166480555hg38UCSC Ensembl
chr3:165812818..166198343hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38385526
hg19385526
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362401
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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