A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160372



Internal ID21506626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130419670..130419742hg38UCSC Ensembl
chr9:133295057..133295129hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603848
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160372
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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