A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229565



Internal ID22371375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64086058..64104614hg38UCSC Ensembl
chr8:64998615..65017171hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3818557
hg1918557
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342344, nssv14342343
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229565
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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