A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592707



Internal ID20965778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80904915..80917664hg38UCSC Ensembl
chr16:80938812..80951561hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3812750
hg1912750
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592707
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