A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229391



Internal ID22371258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63319312..63319366hg38UCSC Ensembl
chr11:63086784..63086838hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1417n152
Supporting Variantsnssv14359797, nssv14359795, nssv14359798, nssv14359796, nssv14359799
SamplesNA19239, HG00731, HG00732, HG00733, HG00513
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229391
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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