A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5136n223



Internal ID22808104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3883949..4174086hg38UCSC Ensembl
chr4:3885676..4175813hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38290138
hg19290138
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6356383, nsv6371566
Samples
Known GenesFAM86EP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5136n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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