A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3242897



Internal ID22375416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6379236..6390589hg38UCSC Ensembl
chr9:6379236..6390589hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3811354
hg1911354
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14343862, nssv14343861, nssv14343859, nssv14343857, nssv14343858, nssv14343860
SamplesHG00512, NA19238, NA19239, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3242897
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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