A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1023n209



Internal ID22827098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21972932..22180934hg38UCSC Ensembl
chr19:22155734..22363736hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38208003
hg19208003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5938160, nsv5944165, nsv5946838
Samples
Known GenesZNF208, ZNF257, ZNF676
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1023n209
Frequency
Sample Size914
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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