A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3232286



Internal ID22372466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168692356..168695795hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383440
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8248n152
Supporting Variantsnssv14332381, nssv14332382, nssv14332385, nssv14332386, nssv14332379, nssv14332383, nssv14332384, nssv14332387, nssv14332380
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3232286
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer