A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154859



Internal ID22085364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:114970843..114980205hg38UCSC Ensembl
Outerchr12:114967297..114980678hg38UCSC Ensembl
Innerchr12:115408648..115418010hg19UCSC Ensembl
Outerchr12:115405102..115418483hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg3813382
hg1913382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv65n97
Supporting Variantsnssv4010301
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154859
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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