A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215434



Internal ID22361773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10754060..10754429hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38370
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14302626, nssv14302625, nssv14302624
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215434
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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