A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5046n223



Internal ID22808014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146356704..146366477hg38UCSC Ensembl
chr3:146074491..146084264hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg389774
hg199774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6356983, nsv6372623
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5046n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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