A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559804



Internal ID22428600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7135332..7135332hg38UCSC Ensembl
chr11:7156563..7156563hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14358094, nssv14358089, nssv14358092, nssv14358090, nssv14358093, nssv14358091
SamplesNA19239, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559804
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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