A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3244758



Internal ID22375950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142832638..142838355hg38UCSC Ensembl
chr8:143914054..143919771hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg385718
hg195718
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14343629
SamplesHG00513
Known GenesGML
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3244758
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