A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211746



Internal ID22359210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93046279..93046601hg38UCSC Ensembl
chr9:95808561..95808883hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348933
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211746
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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