A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608478



Internal ID21556783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169582591..169582591hg38UCSC Ensembl
chr3:169300379..169300379hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124874
SamplesHG03732
Known GenesMECOM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608478
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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