A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1073n209



Internal ID22827148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52619186..52978645hg38UCSC Ensembl
chr19:53122439..53481898hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38359460
hg19359460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5947024, nsv5929398
Samples
Known GenesZNF28, ZNF320, ZNF321P, ZNF468, ZNF600, ZNF611, ZNF702P, ZNF816, ZNF816-ZNF321P, ZNF83
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1073n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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