A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1870n223



Internal ID22804838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63369001..63406900hg38UCSC Ensembl
chr13:63943134..63981033hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3837900
hg1937900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6492201, nsv6483719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1870n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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