A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1240n145



Internal ID22814256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82315540..82318278hg38UCSC Ensembl
chr9:84930455..84933193hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg382739
hg192739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112946, nsv3114573
Samplessample216, sample176
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1240n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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