A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5406229



Internal ID185570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10421255..10421306hg38UCSC Ensembl
chr6:10421488..10421539hg19UCSC Ensembl
Cytoband6p24.3
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 Variantsnssv16979558
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5406229
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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