A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225126



Internal ID22368349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11305692..11310558hg38UCSC Ensembl
chrUn_gl000234:11624..16491hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384867
hg194868
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14301333, nssv14301336, nssv14301334, nssv14301332, nssv14301335, nssv14301337, nssv14301331, nssv14301338, nssv14301330
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)nsv3225126
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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