A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3233269



Internal ID22372715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76109077..76158474hg38UCSC Ensembl
chr6:76818794..76868191hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3849398
hg1949398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7979n152
Supporting Variantsnssv14327925
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3233269
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