A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528721



Internal ID22398111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118421954..118423117hg38UCSC Ensembl
chr11:118292669..118293832hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381164
hg191164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14361326, nssv14361325
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528721
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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