A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140058



Internal ID21482413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102486088..102486218hg38UCSC Ensembl
chr9:105248370..105248500hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595371
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140058
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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