A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401217



Internal ID22459087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113127860..113127964hg38UCSC Ensembl
chr3:112846707..112846811hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5889872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401217
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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