A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413818



Internal ID22471688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150851864..150860003hg38UCSC Ensembl
chr3:150569651..150577790hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg388140
hg198140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413818
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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