A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3066n223



Internal ID22806034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28021168..28021956hg38UCSC Ensembl
chr17:26348194..26348982hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38789
hg19789
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6588019, nsv6578176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3066n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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