A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223033



Internal ID22366921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:35865261..35881355hg38UCSC Ensembl
Outerchr15:36157462..36173556hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3816095
hg1916095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14257911, nssv14258750, nssv14257912
SamplesNA19238, NA19239, NA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223033
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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