A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211129



Internal ID22358793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33176922..33181586hg38UCSC Ensembl
chr19:33667828..33672492hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384665
hg194665
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286334, nssv14286338, nssv14286339, nssv14286331, nssv14286332, nssv14286337, nssv14286335, nssv14286336, nssv14286333
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)nsv3211129
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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