A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665014



Internal ID21613319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17778562..17778562hg38UCSC Ensembl
chr20:17759207..17759207hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116446
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665014
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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