A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559490



Internal ID22428291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82841053..82841053hg38UCSC Ensembl
chr11:82552095..82552095hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14358717
SamplesNA19238
Known GenesPRCP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559490
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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