A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559106



Internal ID22427909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127466083..127466083hg38UCSC Ensembl
chr11:127335978..127335978hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14362164
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559106
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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