A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665974



Internal ID21614279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41806648..41806648hg38UCSC Ensembl
chr21:43226808..43226808hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119366
SamplesNA20509
Known GenesPRDM15
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665974
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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