A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100439



Internal ID21272736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15926902..15936100hg38UCSC Ensembl
Innerchr19:16037712..16046910hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg389199
hg199199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111861
Supporting Variants
Samplessample181
Known GenesCYP4F11
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100439
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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