A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566156



Internal ID16006879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105125040..105188269hg38UCSC Ensembl
Innerchr14:105591377..105654606hg19UCSC Ensembl
Innerchr14:104662422..104725651hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3863230
hg1963230
hg1863230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834732, nssv834733
Samples
Known GenesJAG2, MIR6765, NUDT14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566156
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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