A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7659n223



Internal ID22810627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:25500711..25506739hg38UCSC Ensembl
chr9:25500709..25506737hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg386029
hg196029
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6567081, nsv6561974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7659n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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