A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3299n223



Internal ID22806267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14273501..14343900hg38UCSC Ensembl
chr18:14273500..14343899hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3870400
hg1970400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6533298, nsv6533241, nsv6524564, nsv6516407
Samples
Known GenesCYP4F35P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3299n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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