A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3386n223



Internal ID22806354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61518401..61524600hg38UCSC Ensembl
chr18:59185634..59191833hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6516211, nsv6531704
Samples
Known GenesCDH20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3386n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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