A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093036



Internal ID21466805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80183623..80189643hg38UCSC Ensembl
chr13:80757758..80763778hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg386021
hg196021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602357
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093036
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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