A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254140



Internal ID20821180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15933837..15934205hg38UCSC Ensembl
chr21:17306157..17306525hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599604
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254140
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