A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117058



Internal ID21300324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12499254..12516592hg38UCSC Ensembl
Innerchr10:12541253..12558591hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3817339
hg1917339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088620
Samplessample228
Known GenesCAMK1D
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117058
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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