A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902859



Internal ID22678021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13437484..13445926hg38UCSC Ensembl
chr3:13478984..13487426hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg388443
hg198443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391653
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902859
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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