A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163272



Internal ID21460494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93451376..93451448hg38UCSC Ensembl
chr9:96213658..96213730hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587677
Supporting Variants
SamplesHG02818
Known GenesFAM120AOS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163272
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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