A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1439n209



Internal ID22827514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4030576..4133717hg38UCSC Ensembl
chr3:4072260..4175401hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38103142
hg19103142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5902597, nsv5905423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1439n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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