A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606547



Internal ID21554852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57578465..57578465hg38UCSC Ensembl
chr3:57564192..57564192hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131478
SamplesNA12878
Known GenesARF4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606547
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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