A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154828



Internal ID22085333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:33146857..33172081hg38UCSC Ensembl
Outerchr12:33141726..33175458hg38UCSC Ensembl
Innerchr12:33299791..33325015hg19UCSC Ensembl
Outerchr12:33294660..33328392hg19UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg3833733
hg1933733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009045
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154828
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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