A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115618



Internal ID21298884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12263546..12276542hg38UCSC Ensembl
Innerchr10:12305545..12318541hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3812997
hg1912997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089059
Samplessample77
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115618
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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