A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1546n209



Internal ID22827621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3882887..4174292hg38UCSC Ensembl
chr4:3884614..4176019hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38291406
hg19291406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5894305, nsv5905330, nsv5897384, nsv5887692
Samples
Known GenesFAM86EP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1546n209
Frequency
Sample Size914
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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