A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv47n145



Internal ID22813063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87326447..87332182hg38UCSC Ensembl
chr1:87792130..87797865hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg385736
hg195736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3115753, nsv3110513
Samplessample404, sample263, sample273
Known GenesLMO4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv47n145
Frequency
Sample Size467
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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