A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572468



Internal ID20945539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119814531..119816059hg38UCSC Ensembl
chr8:120826771..120828299hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg381529
hg191529
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277090
Samples
Known GenesTAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572468
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