A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533298



Internal ID20906659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14285901..14340300hg38UCSC Ensembl
chr18:14285900..14340299hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3854400
hg1954400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3299n223
Supporting Variantsnssv18177211
Samples
Known GenesCYP4F35P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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