A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222395



Internal ID22366485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:93730936..93752120hg38UCSC Ensembl
Outerchr9:96493218..96514402hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3821185
hg1921185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282859, nssv14282858, nssv14282860
SamplesHG00731, HG00513, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222395
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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