A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413787



Internal ID22471657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106809420..106857354hg38UCSC Ensembl
chr4:107730577..107778511hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3847935
hg1947935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894118
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413787
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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