A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091402



Internal ID21277331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:87284572..87293655hg38UCSC Ensembl
Innerchr12:87678349..87687432hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg389084
hg199084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117093
Supporting Variants
Samplessample25
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091402
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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