A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419344



Internal ID22477214
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 StatusS
Merged Variantsnsv5964019
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419344
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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