A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv819n145



Internal ID22813835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:163139554..163233298hg38UCSC Ensembl
chr3:162857342..162951086hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3893745
hg1993745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116170, nsv3114180
Samplessample370, sample324
Known GenesCT64
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv819n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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