A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282137



Internal ID20491355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34541241..34561875hg38UCSC Ensembl
chr14:35010447..35031081hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3820635
hg1920635
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755210
Supporting Variants
Samples
Known GenesSNX6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282137
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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