A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213477



Internal ID22360412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33462006..33470934hg38UCSC Ensembl
chr8:33319524..33328452hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg388929
hg198929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340508, nssv14340510, nssv14340509
SamplesNA19238, NA19239, NA19240
Known GenesFUT10
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213477
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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