A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223931



Internal ID22367541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30309862..30309928hg38UCSC Ensembl
chr8:30167378..30167444hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9123n152
Supporting Variantsnssv14340392, nssv14340391
SamplesNA19240, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223931
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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