A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116494



Internal ID21299760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:94871727..94875261hg38UCSC Ensembl
Innerchr12:95265503..95269037hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg383535
hg193535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092388
Samplessample229
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116494
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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