A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112206



Internal ID21295472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100892745..100900040hg38UCSC Ensembl
Innerchr14:101359082..101366377hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg387296
hg197296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095510
Samplessample196
Known GenesMEG8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112206
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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