A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5404474



Internal ID183826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108070703..108070754hg38UCSC Ensembl
chr3:107789550..107789601hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937547
Samples
Known GenesCD47
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5404474
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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