A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218776



Internal ID22364015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68074007..68164345hg38UCSC Ensembl
Outerchr15:68366345..68456683hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3890339
hg1990339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2966n152
Supporting Variantsnssv14258474
SamplesHG00513
Known GenesPIAS1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218776
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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