A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355730



Internal ID22581399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145281398..145281485hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3888
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875007
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355730
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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