A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3714n223



Internal ID22806682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53450080..53568103hg38UCSC Ensembl
chr19:53953334..54071357hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38118024
hg19118024
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6518210, nsv6532109
Samples
Known GenesZNF331, ZNF761, ZNF813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3714n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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