A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561103



Internal ID16001826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132511784..132543723hg38UCSC Ensembl
Innerchr12:133088370..133120309hg19UCSC Ensembl
Innerchr12:131598443..131630382hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3831940
hg1931940
hg1831940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3051n54
Supporting Variantsnssv805913
Samples
Known GenesFBRSL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561103
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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