A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219298



Internal ID22364360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:156034460..156046992hg38UCSC Ensembl
Outerchr6:156355594..156368126hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381464
hg191464
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14278966, nssv14278965
SamplesNA19239, NA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219298
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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