A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566125



Internal ID16006848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104865085..104865817hg38UCSC Ensembl
Innerchr14:105331422..105332154hg19UCSC Ensembl
Innerchr14:104402467..104403199hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38733
hg19733
hg18733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3969n54
Supporting Variantsnssv834692, nssv834691
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566125
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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