A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449055



Internal ID227304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69117498..69155080hg38UCSC Ensembl
chr3:69166649..69204231hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3837583
hg1937583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934046
Samples
Known GenesLMOD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449055
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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