A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116853



Internal ID21504348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35153670..35153670hg38UCSC Ensembl
chr20:33741473..33741473hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671749
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116853
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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