A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224605



Internal ID20791645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1667405..1683364hg38UCSC Ensembl
chr11:1688635..1704594hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3815960
hg1915960
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588417
Supporting Variants
Samples
Known GenesFAM99A, FAM99B, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224605
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00035


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