A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117787



Internal ID21301053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:41162576..41182767hg38UCSC Ensembl
Innerchr12:41556378..41576569hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3820192
hg1920192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv254n145
Supporting Variantsnssv14093926
Samplessample410
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117787
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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