A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3316n223



Internal ID22806284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14354401..14511200hg38UCSC Ensembl
chr18:14354400..14511199hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38156800
hg19156800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6532150, nsv6523791
Samples
Known GenesCXADRP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3316n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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