A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222387



Internal ID22366481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:83865144..83878395hg38UCSC Ensembl
Outerchr15:84533896..84547147hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3813252
hg1913252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3009n152
Supporting Variantsnssv14258829
SamplesNA19238
Known GenesADAMTSL3
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222387
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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