A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218358



Internal ID22363727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:97138773..97162047hg38UCSC Ensembl
Outerchr9:99901055..99924329hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3823275
hg1923275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281248, nssv14281250, nssv14281249
SamplesNA19238, NA19239, NA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218358
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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