A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4823n223



Internal ID22807791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24394401..24435300hg38UCSC Ensembl
chr3:24435892..24476791hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3840900
hg1940900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6373841, nsv6371619
Samples
Known GenesTHRB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4823n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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