A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199079



Internal ID22348715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10572..10967hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38396
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14304941, nssv14304940, nssv14304937, nssv14304936, nssv14304938, nssv14304939
SamplesHG00512, HG00731, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199079
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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