A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117543



Internal ID21410593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60553033..60555556hg38UCSC Ensembl
chr20:59128091..59130614hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382524
hg192524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596876
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117543
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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