A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3712n223



Internal ID22806680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53414823..53512486hg38UCSC Ensembl
chr19:53918076..54015740hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3897664
hg1997665
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6524952, nsv6531396, nsv6531190
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3712n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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