A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569890



Internal ID20942961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120730223..120730908hg38UCSC Ensembl
chr8:121742463..121743148hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7479n223
Supporting Variantsnssv18276056
Samples
Known GenesSNTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569890
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