A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115905



Internal ID21299171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102195357..102211837hg38UCSC Ensembl
Innerchr10:103955114..103971594hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3816481
hg1916481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv176n145
Supporting Variantsnssv14088658, nssv14089813
Samplessample358, sample243
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115905
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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