A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222124



Internal ID20789164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77738048..77738735hg38UCSC Ensembl
chr11:77449093..77449780hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578953
Supporting Variants
Samples
Known GenesRSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222124
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