A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228627



Internal ID22370752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131633687..131633766hg38UCSC Ensembl
chr11:131503581..131503660hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1634n152
Supporting Variantsnssv14362971, nssv14362970
SamplesNA19239, NA19240
Known GenesNTM
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228627
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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