A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281918



Internal ID20491136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110305546..110305546hg38UCSC Ensembl
chr6:110626749..110626749hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760857
Supporting Variants
Samples
Known GenesMETTL24
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281918
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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