A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099687



Internal ID21269616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29611692..29616164hg38UCSC Ensembl
Innerchr19:30102599..30107071hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg384473
hg194473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111667
Supporting Variants
Samplessample141
Known GenesPOP4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099687
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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