A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834646



Internal ID15781916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104863421..104865556hg38UCSC Ensembl
Innerchr14:105329758..105331893hg19UCSC Ensembl
Innerchr14:104400803..104402938hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg382136
hg192136
hg182136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566104
Supporting Variants
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834646
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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