A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422402



Internal ID22480272
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 StatusS
Merged Variantsnsv5896794
Supporting Variants
Samples
Known GenesC3orf20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422402
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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