A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896055



Internal ID22671144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43032980..43033112hg38UCSC Ensembl
chr3:43074472..43074604hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420385
Samples
Known GenesFAM198A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896055
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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