A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111256



Internal ID21294522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100065076..100069391hg38UCSC Ensembl
Innerchr14:100531413..100535728hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384316
hg194316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094131
Samplessample54
Known GenesEVL
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111256
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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