A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116542



Internal ID21495758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34200948..34201023hg38UCSC Ensembl
chr20:32788754..32788829hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600279
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116542
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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