A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427931



Internal ID21085484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28421612..28422501hg38UCSC Ensembl
chr8:28279129..28280018hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166146
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427931
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