A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5616679



Internal ID21564984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43032980..43032980hg38UCSC Ensembl
chr3:43074472..43074472hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139179
SamplesNA19650
Known GenesFAM198A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5616679
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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