A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418191



Internal ID21075744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66683358..66687154hg38UCSC Ensembl
chr8:67595593..67599389hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg383797
hg193797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169421
Samples
Known GenesC8orf44-SGK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418191
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