A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3230273



Internal ID22371844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86247099..86252515hg38UCSC Ensembl
chr11:85958141..85963557hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg385417
hg195417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14359417, nssv14358793, nssv14358792
SamplesHG00731, HG00732, HG00733
Known GenesEED
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3230273
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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