A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv559745



Internal ID16347154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:90528232..90670394hg38UCSC Ensembl
Innerchr12:90922009..91064171hg19UCSC Ensembl
Innerchr12:89446140..89588302hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38142163
hg19142163
hg18142163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv800471
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv559745
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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