A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426000



Internal ID22483870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143230829..143244921hg38UCSC Ensembl
chr4:144151982..144166074hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3814093
hg1914093
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894272
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426000
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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