A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580314



Internal ID20953385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24998247..25024675hg38UCSC Ensembl
chr11:25019793..25046221hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3826429
hg1926429
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222769
Samples
Known GenesLUZP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580314
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