A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558606



Internal ID20931677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23050872..23051570hg38UCSC Ensembl
chr8:22908385..22909083hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7297n223
Supporting Variantsnssv18277489
Samples
Known GenesTNFRSF10B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558606
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