A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647286



Internal ID21839333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40022865..40033183hg38UCSC Ensembl
chr21:41394792..41405110hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3810319
hg1910319
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104052
Supporting Variants
Samples
Known GenesDSCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647286
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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