A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118254



Internal ID21301520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:102236664..102278877hg38UCSC Ensembl
Innerchr12:102630442..102672655hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3842214
hg1942214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093699
Samplessample332
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118254
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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