A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17428281



Internal ID22486151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21957328..21957400hg38UCSC Ensembl
chr4:21958951..21959023hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896571
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17428281
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003


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