A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655828



Internal ID21604133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57915232..57915232hg38UCSC Ensembl
chr17:55992593..55992593hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087763
SamplesNA19239
Known GenesCUEDC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655828
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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