A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1912n223



Internal ID22804880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71226001..71284500hg38UCSC Ensembl
chr13:71800133..71858632hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3858500
hg1958500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6484407, nsv6483424
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1912n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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