A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889872



Internal ID22664893
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 StatusM
Merged Variants
Supporting Variantsnssv17401217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889872
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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