A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561794



Internal ID334763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30607157..30607208hg38UCSC Ensembl
chr3:30648649..30648700hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg382708
hg192708
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930420
Samples
Known GenesTGFBR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561794
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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