A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3376n223



Internal ID22806344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56089201..56131900hg38UCSC Ensembl
chr18:53756432..53799131hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3842700
hg1942700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6520547, nsv6525079
Samples
Known GenesLOC100505474
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3376n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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