A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1139n145



Internal ID22814155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145219396..145225203hg38UCSC Ensembl
chr7:144916489..144922296hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg385808
hg195808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112888, nsv3111574, nsv3115953
Samplessample37, sample373, sample69, sample402, sample421, sample345, sample243, sample364, sample97, sample26, sample168, sample163
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1139n145
Frequency
Sample Size467
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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