A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511441



Internal ID20884769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69705529..69714753hg38UCSC Ensembl
chr16:69739432..69748656hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg389225
hg199225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031231
Samples
Known GenesNQO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511441
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