A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591341



Internal ID20964412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60131101..60131990hg38UCSC Ensembl
chr16:60165005..60165894hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591341
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