A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154810



Internal ID22085315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:11320628..11359557hg38UCSC Ensembl
Outerchr12:11314521..11359597hg38UCSC Ensembl
Innerchr12:11473562..11512491hg19UCSC Ensembl
Outerchr12:11467455..11512531hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3845077
hg1945077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007997
Samples
Known GenesPRB1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154810
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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