A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226842



Internal ID22369511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10954320..10963951hg38UCSC Ensembl
chrUn_gl000241:29748..39379hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg389632
hg199632
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14303266, nssv14302646, nssv14303267, nssv14302645, nssv14303268, nssv14302647, nssv14302649, nssv14302648, nssv14303265
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)nsv3226842
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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