A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223947



Internal ID22367550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:102046029..102135309hg38UCSC Ensembl
Outerchr9:104808311..104897591hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3889281
hg1989281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281265
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223947
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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