A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184481



Internal ID20751521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14286001..14341900hg38UCSC Ensembl
chr18:14286000..14341899hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3855900
hg1955900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533241
Supporting Variants
Samples
Known GenesCYP4F35P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184481
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00125


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