A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669624



Internal ID21617929
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 Variantsdgv4n207
Supporting Variantsnssv17162725
Samples
Known GenesCDK20, SPATA31C2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669624
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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