A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111255



Internal ID21294521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:41162576..41178703hg38UCSC Ensembl
Innerchr12:41556378..41572505hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3816128
hg1916128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv254n145
Supporting Variantsnssv14092559
Samplessample289
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111255
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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