A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214432



Internal ID22361093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:35979139..36004756hg38UCSC Ensembl
Outerchr9:35979136..36004753hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3825618
hg1925618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14281895, nssv14281894
SamplesNA19239, NA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214432
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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