A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5413540



Internal ID192830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:18276645..18276696hg38UCSC Ensembl
chr2:18457911..18457962hg19UCSC Ensembl
Cytoband2p24.2
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 Variantsnssv16910147
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5413540
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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