A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116347



Internal ID21299613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:117905637..117911040hg38UCSC Ensembl
Innerchr6:118226800..118232203hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg385404
hg195404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083877
Samplessample397
Known GenesSLC35F1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116347
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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