A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220408



Internal ID22365110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92024557..92024863hg38UCSC Ensembl
chr9:94786839..94787145hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348896
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220408
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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