A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570844



Internal ID20943915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22432332..22432686hg38UCSC Ensembl
chr8:22289845..22290199hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277476
Samples
Known GenesSLC39A14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570844
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