A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584288



Internal ID20957359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126237239..126238213hg38UCSC Ensembl
chr11:126107134..126108108hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38975
hg19975
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1332n223
Supporting Variantsnssv18220439
Samples
Known GenesFAM118B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584288
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