A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162725



Internal ID21512662
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 StatusS
Merged Variantsnsv5669624
Supporting Variants
Samples
Known GenesCDK20, SPATA31C2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162725
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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