A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9742n152



Internal ID22825445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123976373..123993780hg38UCSC Ensembl
chr9:126738652..126756059hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3817408
hg1917408
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3242008, nsv3244241
SamplesNA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
Single strand sequencing, and assortment analysis
PlatformIllumina HiSeq
Strand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9742n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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