A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578285



Internal ID20951356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58241622..58366294hg38UCSC Ensembl
chr11:58009094..58133767hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38124673
hg19124674
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222745
Samples
Known GenesOR10W1, OR5B17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578285
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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