A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527286



Internal ID22396673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75127461..75127521hg38UCSC Ensembl
chr11:74838506..74838566hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1469n152
Supporting Variantsnssv14357917, nssv14357916, nssv14357915, nssv14357919, nssv14357918, nssv14357914
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527286
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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