A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212457



Internal ID22359702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98393369..98393425hg38UCSC Ensembl
chr9:101155651..101155707hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9680n152
Supporting Variantsnssv14349698
SamplesNA19240
Known GenesGABBR2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212457
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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