A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214345



Internal ID22361024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102631764..102631893hg38UCSC Ensembl
chr8:103643992..103644121hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342202, nssv14342201, nssv14342200
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214345
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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