A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111243



Internal ID21294509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:110131642..110138066hg38UCSC Ensembl
Innerchr12:110569447..110575871hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg386425
hg196425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090345
Samplessample7
Known GenesIFT81
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111243
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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