A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5257n223



Internal ID22808225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46690701..46734300hg38UCSC Ensembl
chr4:46692718..46736317hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3843600
hg1943600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6389701, nsv6380291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5257n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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