A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154822



Internal ID22085327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31108764..31225980hg38UCSC Ensembl
Outerchr12:31104761..31226462hg38UCSC Ensembl
Innerchr12:31261698..31378914hg19UCSC Ensembl
Outerchr12:31257695..31379396hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38121702
hg19121702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv63n97
Supporting Variantsnssv4009039
Samples
Known GenesDDX11
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154822
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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