A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087316



Internal ID21280661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36987297..36992522hg38UCSC Ensembl
Innerchr8:36844815..36850040hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg385226
hg195226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111961
Supporting Variants
Samplessample300
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087316
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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