A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116061



Internal ID21299327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38797704..38827130hg38UCSC Ensembl
Innerchr4:38799325..38828751hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3829427
hg1929427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093562, nssv14092340, nssv14107113
Samplessample3, sample314, sample259
Known GenesTLR1, TLR6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116061
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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