A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620386



Internal ID21568691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45133446..45133446hg38UCSC Ensembl
chr3:45174938..45174938hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38868
hg19868
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119740
SamplesHG00513
Known GenesCDCP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620386
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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