A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5886n223



Internal ID22808854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110123301..110139651hg38UCSC Ensembl
chr5:109459002..109475352hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3816351
hg1916351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6413994, nsv6412098, nsv6410282
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5886n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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