A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011560



Internal ID21920903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22423089..22426724hg38UCSC Ensembl
chr8:22280602..22284237hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg383636
hg193636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559392
Samples
Known GenesSLC39A14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011560
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer