A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622960



Internal ID21571265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46242982..46242982hg38UCSC Ensembl
chr3:46284473..46284473hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128136
SamplesNA19239
Known GenesCCR3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622960
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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