A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092606



Internal ID21280763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:95839013..95843328hg38UCSC Ensembl
Innerchr12:96232791..96237106hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg384316
hg194316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114701
Supporting Variants
Samplessample302
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092606
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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