A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606384



Internal ID21554689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35748204..35748204hg38UCSC Ensembl
chr3:35789696..35789696hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119662
SamplesHG03125
Known GenesARPP21
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606384
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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