A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231848



Internal ID20798888
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 StatusS
Merged Variantsnsv6451254
Supporting Variants
Samples
Known GenesOR1J1, OR1J2, OR1J4, OR1L8, OR1N1, OR1N2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231848
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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