A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528599



Internal ID22397988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21352535..21352802hg38UCSC Ensembl
chr8:21210046..21210313hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340326, nssv14340324, nssv14340325
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528599
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