A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227886



Internal ID22370237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12609650..12615065hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385416
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14302204, nssv14302210, nssv14302207, nssv14302208, nssv14302212, nssv14302205, nssv14302206, nssv14302209, nssv14302211
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)nsv3227886
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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