A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991395



Internal ID21900738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139168368..139172878hg38UCSC Ensembl
chr3:138887210..138891720hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg384511
hg194511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991395
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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