A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118135



Internal ID21301401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:89757214..89763444hg38UCSC Ensembl
Innerchr12:90150991..90157221hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg386231
hg196231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093801
Samplessample366
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118135
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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