A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6019n223



Internal ID22808987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166410701..166422900hg38UCSC Ensembl
chr5:165837706..165849905hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3812200
hg1912200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6409531, nsv6410197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6019n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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