A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451072



Internal ID21108625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124784969..124785471hg38UCSC Ensembl
chr9:127547248..127547750hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232340
Samples
Known GenesOLFML2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451072
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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