A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4983n223



Internal ID22807951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114792701..114834100hg38UCSC Ensembl
chr3:114511548..114552947hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3841400
hg1941400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6364092, nsv6372400
Samples
Known GenesZBTB20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4983n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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