A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278564



Internal ID20845604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68305559..68307641hg38UCSC Ensembl
chr8:69217794..69219876hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg382083
hg192083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565790
Supporting Variants
Samples
Known GenesLOC286189
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278564
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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