A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv483n145



Internal ID22813499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19865283..19868956hg38UCSC Ensembl
chr17:19768596..19772269hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383674
hg193674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112213, nsv3115852
Samplessample214, sample138
Known GenesULK2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv483n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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