A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4928n223



Internal ID22807896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78291995..78297652hg38UCSC Ensembl
chr3:78341145..78346802hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg385658
hg195658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6357592, nsv6360566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4928n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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