A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226471



Internal ID22369260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66253887..66273157hg38UCSC Ensembl
chr9:42248540..42267126hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3819271
hg1918587
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14346789, nssv14346782, nssv14346783, nssv14346784, nssv14346788, nssv14346790, nssv14346785, nssv14346787, nssv14346786
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)nsv3226471
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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