A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1766n223



Internal ID22804734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19817842..19962541hg38UCSC Ensembl
chr13:20391982..20536681hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38144700
hg19144700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6486887, nsv6491642
Samples
Known GenesZMYM2, ZMYM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1766n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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