A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216940



Internal ID22362769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90884716..90884778hg38UCSC Ensembl
chr9:93646998..93647060hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9655n152
Supporting Variantsnssv14348836, nssv14348835, nssv14348837, nssv14348834
SamplesHG00732, HG00733, HG00513, HG00514
Known GenesSYK
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216940
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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