A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212369



Internal ID22359638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:43049879..43089284hg38UCSC Ensembl
Outerchr9:42896016..42933347hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3839406
hg1937332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282896
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212369
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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