A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253034



Internal ID20820074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29451521..29452114hg38UCSC Ensembl
chr21:30823841..30824434hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253034
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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