A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612052



Internal ID21560357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141599751..141599751hg38UCSC Ensembl
chr3:141318593..141318593hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124143
SamplesNA24385
Known GenesRASA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612052
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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