A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225418



Internal ID20792458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133060690..133081168hg38UCSC Ensembl
chr9:135936077..135956555hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3820479
hg1920479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448899
Supporting Variants
Samples
Known GenesCEL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225418
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00502


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