A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231771



Internal ID20798811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90123410..90191700hg38UCSC Ensembl
chr11:89856578..89924868hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3868291
hg1968291
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585443
Supporting Variants
Samples
Known GenesNAALAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231771
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