A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952304



Internal ID22727621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59143893..59143893hg38UCSC Ensembl
chr3:59129619..59129619hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416759
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952304
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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