A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116863



Internal ID21446791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35580687..35580687hg38UCSC Ensembl
chr20:34168609..34168609hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670473
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116863
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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