A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115758



Internal ID21299024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:22743868..22763861hg38UCSC Ensembl
Innerchr12:22896802..22916795hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3819994
hg1919994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091231
Samplessample183
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115758
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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