A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3232666



Internal ID22372565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2167963..2174475hg38UCSC Ensembl
chr19:2167962..2174474hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386513
hg196513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14291118, nssv14291119
SamplesNA19239, NA19240
Known GenesDOT1L
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3232666
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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