A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092388



Internal ID21275892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:94871727..94875261hg38UCSC Ensembl
Innerchr12:95265503..95269037hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg383535
hg193535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116494
Supporting Variants
Samplessample229
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092388
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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