A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668335



Internal ID21616640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59541821..59541821hg38UCSC Ensembl
chr20:58116876..58116876hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117186
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668335
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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