A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv416n206



Internal ID22755720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:60000..87000hg38UCSC Ensembl
chr6:60001..87000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3827001
hg1927000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6141112, nsv6140504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv416n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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