A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560190



Internal ID16000913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:111538972..111542046hg38UCSC Ensembl
Innerchr12:111976776..111979850hg19UCSC Ensembl
Innerchr12:110461159..110464233hg18UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg383075
hg193075
hg183075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2870n54
Supporting Variantsnssv802220, nssv802218, nssv802221, nssv802219
Samples
Known GenesATXN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560190
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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