A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14388207



Internal ID22210789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87372981..87373103hg38UCSC Ensembl
chr16:87406587..87406709hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227919
Supporting Variants
SamplesHG00732
Known GenesFBXO31
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14388207
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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