A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278492



Internal ID20845532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66588436..66589040hg38UCSC Ensembl
chr8:67500671..67501275hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556682
Supporting Variants
Samples
Known GenesMYBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278492
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00023


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