A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556943



Internal ID20930014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107115649..107116613hg38UCSC Ensembl
chr8:108127877..108128841hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38965
hg19965
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556943
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