A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116699



Internal ID21404555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46788837..46788837hg38UCSC Ensembl
chr20:45417476..45417476hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38964
hg19964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665871
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116699
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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