A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490118



Internal ID22548040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197107769..197114993hg38UCSC Ensembl
chr3:196834640..196841864hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg387225
hg197225
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835201
Supporting Variants
Samples
Known GenesDLG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490118
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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