A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3462n223



Internal ID22806430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20386262..20929913hg38UCSC Ensembl
chr19:20497071..21112719hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38543652
hg19615649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6528684, nsv6518301
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF626, ZNF737, ZNF826P, ZNF85
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3462n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer