A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560985



Internal ID20934056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90593406..90594571hg38UCSC Ensembl
chr6:91303125..91304290hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381166
hg191166
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560985
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