A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154824



Internal ID22085329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31125097..31254189hg38UCSC Ensembl
Outerchr12:31116364..31256945hg38UCSC Ensembl
Innerchr12:31278031..31407123hg19UCSC Ensembl
Outerchr12:31269298..31409879hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38140582
hg19140582
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv63n97
Supporting Variantsnssv4009041
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154824
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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