A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153316



Internal ID19201443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:93413053..93419454hg38UCSC Ensembl
Outerchr14:93879399..93885800hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg386402
hg196402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001234
SamplesKWB1
Known GenesUNC79
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153316
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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