A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567514



Internal ID20940585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23104844..23161401hg38UCSC Ensembl
chr8:22962357..23018914hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3856558
hg1956558
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7299n223
Supporting Variantsnssv18277498
Samples
Known GenesTNFRSF10C, TNFRSF10D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567514
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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