A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346509



Internal ID22276016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37552581..37553200hg38UCSC Ensembl
chr9:37552578..37553197hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212624
Supporting Variants
SamplesNA19239
Known GenesFBXO10
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346509
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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