A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565920



Internal ID20938991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138380684..138381118hg38UCSC Ensembl
chr6:138701821..138702255hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272456
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565920
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