A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564058



Internal ID16004781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24302079..24317770hg38UCSC Ensembl
Innerchr14:24771285..24786976hg19UCSC Ensembl
Innerchr14:23841125..23856816hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3815692
hg1915692
hg1815692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv824388
Samples
Known GenesCIDEB, LTB4R, LTB4R2, NOP9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564058
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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