A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420704



Internal ID21078257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66027361..66033358hg38UCSC Ensembl
chr8:66939596..66945593hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg385998
hg195998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232233
Samples
Known GenesDNAJC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420704
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