A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091314



Internal ID21274746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:50280567..50290670hg38UCSC Ensembl
Innerchr12:50674350..50684453hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg3810104
hg1910104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112125
Supporting Variants
Samplessample210
Known GenesLIMA1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091314
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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