A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5675n223



Internal ID22808643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17646506..17796479hg38UCSC Ensembl
chr5:17646615..17796588hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38149974
hg19149974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6376788, nsv6388729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5675n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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