A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219487



Internal ID22364496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95485513..95486717hg38UCSC Ensembl
chr11:95218677..95219881hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381205
hg191205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14360137, nssv14360139, nssv14360140, nssv14360138, nssv14360134, nssv14360133, nssv14360136, nssv14360135, nssv14360141
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219487
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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