A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417716



Internal ID21075269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92767300..92822014hg38UCSC Ensembl
chr8:93779528..93834242hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3854715
hg1954715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236062
Samples
Known GenesFLJ46284
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417716
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