A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218098



Internal ID22363558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19642692..19643041hg38UCSC Ensembl
chr9:19642690..19643039hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14345732, nssv14345731
SamplesNA19238, NA19240
Known GenesSLC24A2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218098
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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