A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3244914



Internal ID22375992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104960294..105038067hg38UCSC Ensembl
chr8:105972522..106050295hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3877774
hg1977774
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342874
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3244914
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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