A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559681



Internal ID22428481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46161938..46161938hg38UCSC Ensembl
chr11:46183489..46183489hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357545, nssv14357546, nssv14358171, nssv14357544, nssv14357547
SamplesHG00512, HG00731, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559681
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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