A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv647n209



Internal ID22826722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105691298..106810442hg38UCSC Ensembl
chr14:106157635..107218676hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381119145
hg191061042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5930755, nsv5945938, nsv5943056, nsv5946828, nsv5934435, nsv5936590, nsv5928065, nsv5931425, nsv5940127, nsv5938444, nsv5939582, nsv5945285, nsv5941497, nsv5927834, nsv5938492, nsv5944219, nsv5943300, nsv5946083
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv647n209
Frequency
Sample Size914
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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