A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5218n223



Internal ID22808186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31642984..31735475hg38UCSC Ensembl
chr4:31644606..31737097hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3892492
hg1992492
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6369809, nsv6358103
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5218n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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