A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1165n209



Internal ID22827240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88860605..90027172hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381166568
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5979550, nsv5968159
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1165n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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