A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4765n223



Internal ID22807733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4006276..4217513hg38UCSC Ensembl
chr3:4047960..4259197hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38211238
hg19211238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6366058, nsv6365204, nsv6369972, nsv6369199, nsv6359156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4765n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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