A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578302



Internal ID20951373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52937802..52937868hg38UCSC Ensembl
chr16:52971714..52971780hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240706
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578302
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