A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092340



Internal ID21277763
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 StatusS
Merged Variantsnsv3116061
Supporting Variants
Samplessample259
Known GenesTLR1, TLR6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092340
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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