A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559457



Internal ID22428258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33880285..33880285hg38UCSC Ensembl
chr11:33901831..33901831hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357631, nssv14357630
SamplesHG00513, HG00514
Known GenesLMO2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559457
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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