A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111885



Internal ID21295151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90957334..90962162hg38UCSC Ensembl
Innerchr10:92717091..92721919hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg384829
hg194829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089023, nssv14088543, nssv14089093, nssv14089082
Samplessample90, sample95, sample59, sample192
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111885
Frequency
Sample Size467
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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