A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669496



Internal ID21617802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36320000..36320000hg38UCSC Ensembl
chr20:34948403..34948403hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116878
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669496
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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