A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv448n145



Internal ID22813464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65142459..65143403hg38UCSC Ensembl
chr16:65176362..65177306hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114468, nsv3116668, nsv3110752
Samplessample75, sample182, sample112, sample331, sample283
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv448n145
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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