A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3530066



Internal ID22399457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112331777..112331915hg38UCSC Ensembl
chr11:112202500..112202638hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14361556, nssv14361555
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3530066
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