A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588937



Internal ID20962008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102326802..102327488hg38UCSC Ensembl
chr11:102197533..102198219hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225738
Samples
Known GenesBIRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588937
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