A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092491



Internal ID21278039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:128472019..128488920hg38UCSC Ensembl
Innerchr12:128956564..128973465hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3816902
hg1916902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114469
Supporting Variants
Samplessample263
Known GenesTMEM132C
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092491
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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