A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560962



Internal ID16001685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132149229..132150681hg38UCSC Ensembl
Innerchr12:132633774..132635226hg19UCSC Ensembl
Innerchr12:131199727..131201179hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg381453
hg191453
hg181453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3017n54
Supporting Variantsnssv805503
Samples
Known GenesNOC4L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560962
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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