A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428501



Internal ID21086054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128262501..128274400hg38UCSC Ensembl
chr8:129274747..129286646hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3811900
hg1911900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163842
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428501
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