A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116496



Internal ID21467751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22520993..22520993hg38UCSC Ensembl
chr20:22501631..22501631hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg386061
hg196061
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669564
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116496
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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