A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092862



Internal ID21270056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:113739260..113756677hg38UCSC Ensembl
Innerchr12:114177065..114194482hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3817418
hg1917418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114097
Supporting Variants
Samplessample146
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092862
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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