A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154855



Internal ID22085360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:110796150..110797921hg38UCSC Ensembl
Outerchr12:110788037..110800645hg38UCSC Ensembl
Innerchr12:111233954..111235725hg19UCSC Ensembl
Outerchr12:111225842..111238449hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3812609
hg1912608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010297
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154855
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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