A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv669n145



Internal ID22813685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:225122422..225124356hg38UCSC Ensembl
chr2:225987139..225989073hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg381935
hg191935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114381, nsv3115222
Samplessample118, sample147, sample10
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv669n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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