A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400413



Internal ID22458283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47604073..47604126hg38UCSC Ensembl
chr19:48107330..48107383hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932007
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400413
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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