A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv414n206



Internal ID22755718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181353000..181368000hg38UCSC Ensembl
chr5:180780001..180795001hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3815001
hg1915001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6141277, nsv6140866
Samples
Known GenesOR4F16, OR4F29, OR4F3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv414n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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