A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896794



Internal ID22671890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14688306..14689775hg38UCSC Ensembl
chr3:14729813..14731282hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381470
hg191470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422402
Samples
Known GenesC3orf20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896794
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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