A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1836n223



Internal ID22804804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53657601..53665700hg38UCSC Ensembl
chr13:54231736..54239835hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg388100
hg198100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6480702, nsv6488709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1836n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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