A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085277



Internal ID21271320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:78154477..78163722hg38UCSC Ensembl
Innerchr8:79066712..79075957hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg389246
hg199246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117819
Supporting Variants
Samplessample162
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085277
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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