A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218488



Internal ID22363811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:98262964..98303123hg38UCSC Ensembl
Outerchr15:98806193..98846352hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3840160
hg1940160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258460, nssv14258462, nssv14258461
SamplesHG00512, HG00732, HG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218488
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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