A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576465



Internal ID20949536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65028812..65029285hg38UCSC Ensembl
chr11:64796284..64796757hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233510
Samples
Known GenesARL2-SNX15, SNX15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576465
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