A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161959



Internal ID21482871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33585823..33588913hg38UCSC Ensembl
chr9:33585821..33588911hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383091
hg193091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604143
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161959
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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