A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv654n209



Internal ID22826729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105742107..105774734hg38UCSC Ensembl
chr14:106208444..106241071hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3832628
hg1932628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5927936, nsv5935485, nsv5937062, nsv5943385, nsv5929311, nsv5938403
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv654n209
Frequency
Sample Size914
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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