A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229819



Internal ID22371540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138279608..138282592hg38UCSC Ensembl
chr11:125086..128088hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382985
hg193003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350233, nssv14349615, nssv14349616, nssv14350239, nssv14350236, nssv14350234, nssv14350237, nssv14350238, nssv14350235
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesLINC01001
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229819
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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