A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528583



Internal ID22397972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134046061..134046151hg38UCSC Ensembl
chr11:133915956..133916046hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1648n152
Supporting Variantsnssv14363033, nssv14363034, nssv14363035
SamplesNA19238, NA19240, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528583
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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