A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3711n223



Internal ID22806679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53414435..53503378hg38UCSC Ensembl
chr19:53917688..54006632hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3888944
hg1988945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6529575, nsv6527082
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3711n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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