A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955471



Internal ID22730671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28798672..28798672hg38UCSC Ensembl
chr3:28840163..28840163hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955471
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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