A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4851n223



Internal ID22807819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41268648..41783953hg38UCSC Ensembl
chr3:41310139..41825445hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38515306
hg19515307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6358158, nsv6369899
Samples
Known GenesULK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4851n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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