A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv759n145



Internal ID22813775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36590528..36595494hg38UCSC Ensembl
chr3:36632020..36636986hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg384967
hg194967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114273, nsv3113867
Samplessample54, sample295
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv759n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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