A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593113



Internal ID20966184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59562944..59563635hg38UCSC Ensembl
chr11:59330417..59331108hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593113
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