A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560154



Internal ID16347563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:110281203..110284827hg38UCSC Ensembl
Innerchr12:110719008..110722632hg19UCSC Ensembl
Innerchr12:109203391..109207015hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg383625
hg193625
hg183625
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv802002
Samples
Known GenesATP2A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560154
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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