A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113790



Internal ID21297056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121275085..121285274hg38UCSC Ensembl
Innerchr6:121596231..121606420hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3810190
hg1910190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14082828
Samplessample7
Known GenesTBC1D32
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113790
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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