A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101469



Internal ID21283859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33901476..33908185hg38UCSC Ensembl
Innerchr19:34392381..34399090hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg386710
hg196710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113904
Supporting Variants
Samplessample350
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101469
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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