A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv402n206



Internal ID22755706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69377464..69377682hg38UCSC Ensembl
chr5:68673291..68673509hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5458429, nsv5472201
Samples
Known GenesRAD17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv402n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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