A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221948



Internal ID20788988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62756132..62756741hg38UCSC Ensembl
chr11:62523604..62524213hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576944
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221948
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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