A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572254



Internal ID20945325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85907234..86134252hg38UCSC Ensembl
chr8:86919463..87146481hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38227019
hg19227019
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278920
Samples
Known GenesATP6V0D2, PSKH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572254
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