A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442876



Internal ID221289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131358877..131358932hg38UCSC Ensembl
chr3:131077721..131077776hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939846
Samples
Known GenesLOC339874
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442876
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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