A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5410278



Internal ID189595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155205091..155205098hg38UCSC Ensembl
chr3:154922880..154922887hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5410278
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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