A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664812



Internal ID21613119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32332477..32332477hg38UCSC Ensembl
chr21:33704786..33704786hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118884
SamplesHG03125
Known GenesURB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664812
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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