A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116012



Internal ID21299278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:82675142..82682252hg38UCSC Ensembl
Innerchr12:83068921..83076031hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg387111
hg197111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093723
Samplessample344
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116012
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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