A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217659



Internal ID20784699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65386201..65398200hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3812000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455340
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217659
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.46443


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