A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446790



Internal ID225108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197121140..197122315hg38UCSC Ensembl
chr3:196848011..196849186hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381176
hg191176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16946046
Samples
Known GenesDLG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5446790
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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