A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015485



Internal ID21924828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181095722..181183649hg38UCSC Ensembl
chr5:180522722..180610649hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3887928
hg1987928
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577174
Samples
Known GenesOR2V1, OR2V2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015485
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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