A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559209



Internal ID16346618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:66761830..66783012hg38UCSC Ensembl
Innerchr12:67155610..67176792hg19UCSC Ensembl
Innerchr12:65441877..65463059hg18UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3821183
hg1921183
hg1821183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv797558
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559209
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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