A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv763n145



Internal ID22813779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68579786..68591077hg38UCSC Ensembl
chr3:68628937..68640228hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3811292
hg1911292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114104, nsv3112565
Samplessample164, sample4
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv763n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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