A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670990



Internal ID21619295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18708207..18708207hg38UCSC Ensembl
chr20:18688851..18688851hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116232, nssv17116231
SamplesNA19650, NA19239
Known GenesDTD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670990
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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