A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906623



Internal ID22681825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45938284..45942636hg38UCSC Ensembl
chr3:45979776..45984128hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384353
hg194353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427671
Samples
Known GenesFYCO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906623
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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