A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115588



Internal ID21509346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1813918..1814856hg38UCSC Ensembl
chr20:1794564..1795502hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592797
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115588
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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