A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591143



Internal ID20964214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71085626..71087283hg38UCSC Ensembl
chr17:69081767..69083424hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381658
hg191658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591143
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