A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3249845



Internal ID22377383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:85985643..86024991hg38UCSC Ensembl
Outerchr15:86528874..86568222hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg381608
hg191608
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258860, nssv14258862, nssv14258856, nssv14258859, nssv14258861, nssv14258858, nssv14258857, nssv14258854, nssv14258855
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3249845
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer