A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527395



Internal ID22396781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98238007..98238822hg38UCSC Ensembl
chr9:101000289..101001104hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349680, nssv14349681, nssv14349682
SamplesNA19238, NA19239, NA19240
Known GenesTBC1D2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527395
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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