A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560935



Internal ID16001658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132134511..132150976hg38UCSC Ensembl
Innerchr12:132619056..132635521hg19UCSC Ensembl
Innerchr12:131185009..131201474hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3816466
hg1916466
hg1816466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv805450
Samples
Known GenesDDX51, NOC4L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560935
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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