A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429696



Internal ID208535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62389827..62389878hg38UCSC Ensembl
chr15:62682026..62682077hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429696
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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