A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278703



Internal ID20845743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74175660..74183141hg38UCSC Ensembl
chr8:75087895..75095376hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg387482
hg197482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278703
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.01356


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer