A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214382



Internal ID22361054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3131531..3131591hg38UCSC Ensembl
chr11:3152761..3152821hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1242n152
Supporting Variantsnssv14357298, nssv14357297, nssv14357296
SamplesNA19238, NA19239, NA19240
Known GenesOSBPL5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214382
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