A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278693



Internal ID20845733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73974185..73974902hg38UCSC Ensembl
chr8:74886420..74887137hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558334
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278693
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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