A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116028



Internal ID21299294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94622856..94630490hg38UCSC Ensembl
Innerchr8:95635084..95642718hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg387635
hg197635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088249, nssv14088180
Samplessample369, sample387
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116028
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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