A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085918



Internal ID21289858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88734760..88830567hg38UCSC Ensembl
Innerchr8:89746989..89842796hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3895808
hg1995808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112430
Supporting Variants
Samplessample52
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085918
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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