A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214077



Internal ID22360833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:114120124..114135265hg38UCSC Ensembl
Outerchr9:116882404..116897545hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3815142
hg1915142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282862
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214077
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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