A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3234094



Internal ID22372930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118499582..118506593hg38UCSC Ensembl
chr9:121261860..121268871hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg387012
hg197012
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349165
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3234094
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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