A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5654n223



Internal ID22808622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17288997..17298823hg38UCSC Ensembl
chr5:17289106..17298932hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg389827
hg199827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6379345, nsv6387457
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5654n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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