A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210437



Internal ID20777477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24274501..24284300hg38UCSC Ensembl
chr3:24315992..24325791hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg389800
hg199800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366441
Supporting Variants
Samples
Known GenesTHRB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210437
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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