A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232340



Internal ID20799380
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 StatusS
Merged Variantsnsv6451072
Supporting Variants
Samples
Known GenesOLFML2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232340
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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