A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278452



Internal ID20845492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65610204..65610785hg38UCSC Ensembl
chr8:66522439..66523020hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565281
Supporting Variants
Samples
Known GenesARMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278452
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0007


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