A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2060n223



Internal ID22805028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21847221..22496897hg38UCSC Ensembl
chr14:22315403..22965882hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38649677
hg19650480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6493820, nsv6483985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2060n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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