A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116643



Internal ID21299909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:25485024..25489526hg38UCSC Ensembl
Innerchr14:25954230..25958732hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg384503
hg194503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv321n145
Supporting Variantsnssv14094243, nssv14095377, nssv14094102, nssv14096275, nssv14094159
Samplessample69, sample146, sample256, sample96, sample45
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116643
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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