A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2294n223



Internal ID22805262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105740005..105773003hg38UCSC Ensembl
chr14:106206342..106239340hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3832999
hg1932999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6512502, nsv6504609, nsv6505474, nsv6505610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2294n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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