A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161477



Internal ID21512807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20267049..20291167hg38UCSC Ensembl
chr9:20267047..20291165hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3824119
hg1924119
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669463
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161477
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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