A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090345



Internal ID21291182
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 StatusS
Merged Variantsnsv3111243
Supporting Variants
Samplessample7
Known GenesIFT81
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090345
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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