A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561119



Internal ID20934190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166859710..166860111hg38UCSC Ensembl
chr5:166286715..166287116hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267560
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561119
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