A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419723



Internal ID22477593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157888189..157898803hg38UCSC Ensembl
chr4:158809341..158819955hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3810615
hg1910615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907369
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419723
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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