A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162726



Internal ID21412374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87942698..88110273hg38UCSC Ensembl
chr9:90557613..90725188hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38167576
hg19167576
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668795
Supporting Variants
SamplesHG00513
Known GenesCDK20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162726
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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