A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3385n223



Internal ID22806353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61517801..61521816hg38UCSC Ensembl
chr18:59185034..59189049hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg384016
hg194016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6519564, nsv6534224
Samples
Known GenesCDH20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3385n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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