A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278486



Internal ID20845526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66464085..66476565hg38UCSC Ensembl
chr8:67376320..67388800hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3812481
hg1912481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558450
Supporting Variants
Samples
Known GenesADHFE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278486
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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