A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576278



Internal ID20949349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47803999..47805334hg38UCSC Ensembl
chr11:47825551..47826886hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381336
hg191336
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235529
Samples
Known GenesNUP160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576278
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