A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220986



Internal ID22365519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10751732..10751912hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38181
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14302621, nssv14302622, nssv14302623
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220986
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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