A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564151



Internal ID16351560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28100578..28144861hg38UCSC Ensembl
Innerchr14:28569784..28614067hg19UCSC Ensembl
Innerchr14:27639535..27683818hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3844284
hg1944284
hg1844284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3600n54
Supporting Variantsnssv1149489, nssv825091
SamplesNINDS_173
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564151
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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