A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220085



Internal ID22364895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18420626..18420748hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2153n152
Supporting Variantsnssv14366066, nssv14366063, nssv14366067, nssv14366064, nssv14366068, nssv14366065
SamplesHG00512, NA19238, HG00731, HG00732, HG00733, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220085
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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