A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086013



Internal ID21273766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:59729804..59760128hg38UCSC Ensembl
Innerchr8:60642363..60672687hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3830325
hg1930325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115843
Supporting Variants
Samplessample196
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086013
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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