A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556544



Internal ID20929615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100143823..100144651hg38UCSC Ensembl
chr8:101156051..101156879hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38829
hg19829
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275878
Samples
Known GenesFBXO43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556544
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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