A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226409



Internal ID22369219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:108982766..108982833hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1988n152
Supporting Variantsnssv14366302, nssv14366305, nssv14366304, nssv14366303, nssv14366306
SamplesNA19238, HG00731, HG00732, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226409
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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