A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111787



Internal ID21295053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36573238..36574590hg38UCSC Ensembl
Innerchr14:37042443..37043795hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg381353
hg191353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094160
Samplessample69
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111787
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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