A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5398n223



Internal ID22808366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106678401..106703700hg38UCSC Ensembl
chr4:107599558..107624857hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3825300
hg1925300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6395291, nsv6395359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5398n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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