A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590791



Internal ID20963862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96948011..97233407hg38UCSC Ensembl
chr11:96819011..97104407hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38285397
hg19285397
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224193
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590791
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