A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417185



Internal ID21074738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27224025..27233542hg38UCSC Ensembl
chr8:27081542..27091059hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg389518
hg199518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166105
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417185
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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