A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834645



Internal ID15781915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104863421..104865448hg38UCSC Ensembl
Innerchr14:105329758..105331785hg19UCSC Ensembl
Innerchr14:104400803..104402830hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg382028
hg192028
hg182028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566103
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)nssv834645
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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