A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964019



Internal ID22738954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47482454..47482454hg38UCSC Ensembl
chr4:47484471..47484471hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964019
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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