A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278301



Internal ID20845341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56068334..56068883hg38UCSC Ensembl
chr8:56980893..56981442hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558497
Supporting Variants
Samples
Known GenesRPS20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278301
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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