A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5410284



Internal ID189601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170718614..170718665hg38UCSC Ensembl
chr3:170436403..170436454hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5410284
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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