A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112011



Internal ID21295277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:65465706..65470661hg38UCSC Ensembl
Innerchr12:65859486..65864441hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg384956
hg194956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093769
Samplessample360
Known GenesMSRB3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112011
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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