A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114394



Internal ID21297660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86096489..86122380hg38UCSC Ensembl
Innerchr10:87856246..87882137hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3825892
hg1925892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088626
Samplessample229
Known GenesGRID1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114394
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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