A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568691



Internal ID20941762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24976197..26190585hg38UCSC Ensembl
chr8:24833711..26048101hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg381214389
hg191214391
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277536
Samples
Known GenesCDCA2, DOCK5, EBF2, GNRH1, KCTD9, MIR6876
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568691
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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