A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140866



Internal ID340060
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 Variantsdgv414n206
Supporting Variantsnssv16977911
Samples
Known GenesOR4F16, OR4F29, OR4F3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140866
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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