A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5412814



Internal ID192115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149040174..149040225hg38UCSC Ensembl
chr3:148757961..148758012hg19UCSC Ensembl
Cytoband3q24
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 Variantsnssv16940806
Samples
Known GenesHLTF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5412814
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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