A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv671n209



Internal ID22826746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105862654..106666043hg38UCSC Ensembl
chr14:106328864..107122059hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38803390
hg19793196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5931309, nsv5938840, nsv5946696, nsv5939730, nsv5944737, nsv5929603, nsv5928146, nsv5937068, nsv5928176, nsv5944033, nsv5941323, nsv5941077, nsv5933466, nsv5931113, nsv5944042, nsv5939722, nsv5932104, nsv5930189, nsv5935698, nsv5932865, nsv5935344, nsv5937146, nsv5929845, nsv5931280, nsv5943155, nsv5940600, nsv5935737, nsv5932958, nsv5934867, nsv5942599, nsv5927675
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv671n209
Frequency
Sample Size914
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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