A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451254



Internal ID21108807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122410501..122598500hg38UCSC Ensembl
chr9:125172780..125360779hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38188000
hg19188000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231848
Samples
Known GenesOR1J1, OR1J2, OR1J4, OR1L8, OR1N1, OR1N2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451254
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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