A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095441



Internal ID21271736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86935361..86936919hg38UCSC Ensembl
Innerchr14:87401705..87403263hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg381559
hg191559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117289
Supporting Variants
Samplessample168
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095441
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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