A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211449



Internal ID22359009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60516173..60516237hg38UCSC Ensembl
chr15:60808372..60808436hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2949n152
Supporting Variantsnssv14386553, nssv14374170, nssv14373419
SamplesNA19238, HG00732, NA19240
Known GenesRORA
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211449
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