A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437514



Internal ID21095067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122541346..122647696hg38UCSC Ensembl
chr9:125303625..125409975hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38106351
hg19106351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236466
Samples
Known GenesOR1B1, OR1L8, OR1N2, OR1Q1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437514
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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