A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218404



Internal ID22363755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:2900061..2933831hg38UCSC Ensembl
Outerchr9:2900061..2933831hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3833771
hg1933771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282878
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218404
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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