A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4n207



Internal ID22815255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87933867..88157581hg38UCSC Ensembl
chr9:90548782..90772496hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38223715
hg19223715
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5669624, nsv5668795
SamplesHG00513
Known GenesCDK20, SPATA31C2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)dgv4n207
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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