A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560119



Internal ID16000842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:109702208..109714639hg38UCSC Ensembl
Innerchr12:110140013..110152444hg19UCSC Ensembl
Innerchr12:108624396..108636827hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3812432
hg1912432
hg1812432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2856n54
Supporting Variantsnssv801936
Samples
Known GenesFAM222A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560119
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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