A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431332



Internal ID21088885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28881301..28890300hg38UCSC Ensembl
chr8:28738818..28747817hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225322
Samples
Known GenesINTS9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431332
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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