A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560959



Internal ID16001682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132149124..132150007hg38UCSC Ensembl
Innerchr12:132633669..132634552hg19UCSC Ensembl
Innerchr12:131199622..131200505hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38884
hg19884
hg18884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3016n54
Supporting Variantsnssv805500
Samples
Known GenesNOC4L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560959
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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