A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112354



Internal ID21295620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62666769..62678257hg38UCSC Ensembl
Innerchr14:63133487..63144975hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3811489
hg1911489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095320
Samplessample126
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112354
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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