A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569706



Internal ID20942777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69599622..69600358hg38UCSC Ensembl
chr6:70309514..70310250hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569706
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