A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3424n223



Internal ID22806392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4852984..4900519hg38UCSC Ensembl
chr19:4852996..4900531hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3847536
hg1947536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6516954, nsv6529009
Samples
Known GenesARRDC5, PLIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3424n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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