A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114030



Internal ID21297296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10051762..10057019hg38UCSC Ensembl
Innerchr8:9909272..9914529hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg385258
hg195258
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087205
Samplessample360
Known GenesMSRA
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114030
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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