A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1800n223



Internal ID22804768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34982201..34988100hg38UCSC Ensembl
chr13:35556338..35562237hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6494974, nsv6487861
Samples
Known GenesNBEA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1800n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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