A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281284



Internal ID20490502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211609091..211609091hg38UCSC Ensembl
chr1:211782433..211782433hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281284
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