A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665535



Internal ID21613840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46228815..46228815hg38UCSC Ensembl
chr21:47648729..47648729hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130992
SamplesHG00513
Known GenesLSS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665535
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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