A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499886



Internal ID20873111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67054916..67064368hg38UCSC Ensembl
chr16:67088819..67098271hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg389453
hg199453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031328
Samples
Known GenesCBFB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499886
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